Micheliolide derivatives, methods for their preparation and their use as anticancer and antiinflammatory agents

ABSTRACT

The present invention relates to derivatives of the sesquiterpene lactone micheliolide, methods and compositions for their preparation, and methods for using the micheliolide derivatives in pharmaceutical compositions as anticancer and anti-inflammatory agents. The invention also relates to methods for producing micheliolide derivatives modified at positions C2 and C14. The invention also relates to methods for producing parthenolide derivatives modified at positions C2 and C14 in conjunction with modifications at position C13, via chemoenzymatic methods. The invention further relates to methods for using parthenolide derivatives for treating cancer and inflammatory diseases.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is the U.S. national phase application filed under 35 U.S.C. § 371 claiming priority to International Patent Application No. PCT/US2018/046856, filed Aug. 17, 2018, which is entitled to priority under 35 U.S.C. § 119(e) to U.S. Provisional Patent Application Ser. No. 62/547,806, filed Aug. 19, 2017, the disclosures of which are incorporated herein by reference in their entireties.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

This invention was made with government support under GM095628 awarded by National Institutes of Health. The government has certain rights in the invention.

1. TECHNICAL FIELD

The present invention relates to derivatives of the sesquiterpene lactone micheliolide, methods and compositions for their preparation, and methods for using the micheliolide derivatives in pharmaceutical compositions as anticancer and anti-inflammatory agents. The invention also relates to methods for producing micheliolide derivatives modified at positions C2 and C14. The invention also relates to methods for producing parthenolide derivatives modified at positions C2 and C14 in conjunction with modifications at position C13, via chemoenzymatic methods. The invention further relates to methods for using parthenolide derivatives for treating cancer and inflammatory diseases.

2. BACKGROUND OF THE INVENTION

Sesquiterpene lactones (SL) are a diverse family of plant derived natural products with promising inflammatory and anticancer activity. Parthenolide (PTL) is a well-studied SL found in various genera of the Asteraceae and Magnoliaceae family. Parthenolide was found to exhibit a broad spectrum of biological properties, which include anti-inflammatory (Merfort 2011), antitumor (Ghantous, Gali-Muhtasib et al. 2010; Merfort 2011; Janecka, Wyrebska et al. 2012; Kreuger, Grootjans et al. 2012), antiviral (Hwang, Chang et al. 2006), and antileishmanic (Tiuman, Ueda-Nakamura et al. 2005) activity. The anti-inflammatory properties of parthenolide has been associated to its ability to inhibit the NF-κB transcription factor (Hehner, Heinrich et al. 1998; Garcia-Pineres, Castro et al. 2001; Garcia-Pineres, Lindenmeyer et al. 2004), which plays a prevalent role in regulating inflammatory responses (Baeuerle and Henkel 1994) as well as inhibition of other cellular mechanisms involved in inflammation, such as prostaglandin synthesis and IL-1α expression (Hwang, Fischer et al. 1996) and activation of the NLRP-3 inflammasome (Juliana, Femandes-Alnemri et al. 2010). Pharmacological inhibition of NF-κB activation, such as that induced by parthenolide, has been recognized as an important strategy for the treatment of a variety of inflammation-related pathologies, including toxic shock, asthma, and rheumatoid arthritis (Barnes and Adcock 1997; Barnes and Larin 1997). Parthenolide has been identified as the major active ingredient of the medicinal herb feverfew (Tanacetum parthenium), which has found use in the traditional medicine for the treatment of pain, migraine, and rheumatoid arthritis (Heptinstall, White et al. 1985; Knight 1995).

A growing number of studies over the past decade have demonstrated the therapeutic potential of parthenolide also as an anticancer agent. In particular, PTL has emerged as a very promising antileukemic agent owing to its ability to induce robust apoptosis in primary acute myeloid leukemic (AML) cells while exhibiting minimal toxicity toward normal hematopoietic cells (Guzman, Karnischky et al. 2004; Guzman, Rossi et al. 2005; Guzman, Rossi et al. 2006). Most notably, PTL was found to be equally effective amongst all subpopulations found within primary AML specimens, including the so-called leukemia stem cells (LSCs). LSCs typically occur in a quiescent state, which reduces their responsiveness to conventional chemotherapeutic agents that kill actively cycling cells (Holyoake, Jiang et al. 1999; Costello, Mallet et al. 2000; Graham, Jorgensen et al. 2002; Guzman, Swiderski et al. 2002; Guan, Gerhard et al. 2003). Thus, in addition to being involved in the genesis of AML (Lapidot, Sirard et al. 1994; Bonnet and Dick 1997; Cox, Evely et al. 2004), LSCs are believed to play a major role also in clinical relapse of AML patients following traditional chemotherapy (Killmann 1991; van Rhenen, Feller et al. 2005). Thus, the LSC-targeting ability of PTL makes this compound a particularly interesting candidate toward the development of therapeutics for the treatment of AML as well as of other hematologic malignancies.

In addition to AML, PTL has demonstrated activity against numerous other types of cancer. Indeed, recent studies showed that PTL exhibits notable antitumor properties also against breast (Patel, Nozaki et al. 2000; Nakshatri, Rice et al. 2004; Sweeney, Mehrotra et al. 2005; Liu, Lu et al. 2008; Wyrebska, Gach et al. 2012), lung (Zhang, Qiu et al. 2009; Estabrook, Chin-Sinex et al. 2011; Shanmugam, Kusumanchi et al. 2011), prostate (Sun, St Clair et al. 2007; Kawasaki, Hurt et al. 2009; Shanmugam, Kusumanchi et al. 2010; Sun, St Clair et al. 2010), blood (Steele, Jones et al. 2006; Wang, Adachi et al. 2006; Suvannasankha, Crean et al. 2008; Li, Zhang et al. 2012), colon (Zhang, Ong et al. 2004), bladder (Cheng and Xie 2011), liver (Wen, You et al. 2002; Park, Liu et al. 2005; Ralstin, Gage et al. 2006; Kim, Kim et al. 2012), skin (Won, Ong et al. 2004; Won, Ong et al. 2005; Lesiak, Koprowska et al. 2010), brain (Anderson and Bejcek 2008; Zanotto-Filho, Braganhol et al. 2011), pancreas (Kim, Liu et al. 2005; Yip-Schneider, Nakshatri et al. 2005; Yip-Schneider, Wu et al. 2008; Wang, Adachi et al. 2009; Holcomb, Yip-Schneider et al. 2012), kidney (Oka, Nishimura et al. 2007), and bone (Idris, Libouban et al. 2009) cancer.

The anticancer activity of PTL has been primarily linked to its inhibitory activity on NF-κB as this transcription factor controls multiple cellular processes in cancer, including inflammation, transformation, proliferation, angiogenesis, invasion, metastasis, chemoresistance, and radioresistance (Kreuger, Grootjans et al. 2012). However, additional and/or alternative mechanisms of action contribute to PTL anticancer activity, which include activation of p53 (Gopal, Chanchorn et al. 2009), induction of oxidative stress (Wen, You et al. 2002; Zhang, Ong et al. 2004; Wang, Adachi et al. 2006; Sun, St Clair et al. 2010; Shanmugam, Kusumanchi et al. 2011), inhibition of JNK (Nakshatri, Rice et al. 2004) activation of proapoptotic Bcl-2 family members (Zhang, Ong et al. 2004), modulation of exofacial thiols (Skalska, Brookes et al. 2009), and alteration of epigenetic mechanisms via inhibition of DNA methylation (Liu, Liu et al. 2009) and histone deacetylase activity (Gopal, Arora et al. 2007).

From a structure-activity standpoint, the α-methylene-γ-lactone moiety was found to be critically important for parthenolide pharmacological properties, as reduction of the α,β-unsaturated lactone to give 11,13-dehydroparthenolide results in complete loss of activity (Kwok, Koh et al. 2001; Hwang, Chang et al. 2006; Neelakantan, Nasim et al. 2009). The key functional role of this structural moiety is largely related to its ability to react with nucleophilic sulphydryl groups in the cellular components (e.g., enzymes, proteins, glutathione) targeted by PTL (Garcia-Pineres, Castro et al. 2001; Kwok, Koh et al. 2001; Garcia-Pineres, Lindenmeyer et al. 2004; Skalska, Brookes et al. 2009). Despite its interesting biological properties, PTL suffers from a number of drawbacks which include its scarce water-solubility and chemical instability upon exposure to acids (Castaneda-Acosta, Fischer et al. 1993; Neukirch, Kaneider et al. 2003; Nasim and Crooks 2008). These limitations complicate the development and application of PTL analogs as therapeutic agents.

Micheliolide (MCL, 1) is a guaianolide sesquiterpene lactone isolated from Michelia compressa [Ogura, M.; Cordell, G. A.; Farnsworth, N. R. Anticancer sesquiterpene lactones of Michelia compressa (magnoliaceae). Phytochemistry 1978, 17, 957-961] and Michelia champaca [Jacobsson, U.; Kumar, V.; Saminathan, S. Sesquiterpene lactones from Michelia champaca. Phytochemistry 1995, 39, 839-843]. MCL was recently found to possess antileukemic properties comparable to PTL (Zhang, Q.; Lu, Y.; Ding, Y.; Zhai, J.; Ji, Q.; Ma, W.; Yang, M.; Fan, H.; Long, J.; Tong, Z.; Shi, Y.; Jia, Y.; Han, B.; Zhang, W.; Qiu, C.; Ma, X.; Li, Q.; Shi, Q.; Zhang, H.; Li, D.; Zhang, J.; Lin, J.; Li, L.-Y.; Gao, Y.; Chen, Y. J. Med. Chem. 2012, 55, 8757; An, Y.; Guo, W.; Li, L.; Xu, C.; Yang, D.; Wang, S.; Lu, Y.; Zhang, Q.; Zhai, J.; Fan, H.; Qiu, C.; Qi, J.; Chen, Y.; Yuan, S. PLoS One 2015, 10, e0116202]. As previously done in the case of PTL (Guzman, Rossi et al. 2006; Hwang, Chang et al. 2006; Nasim and Crooks 2008; Han, Barrios et al. 2009; Neelakantan, Nasim et al. 2009; Woods, Mo et al. 2011), efforts toward the development of MCL derivatives with potentially improved pharmacological properties have involved the addition of dimethylamine to the reactive α-methylene-γ-lactone moiety, resulting in the C13-dimethylamino adduct of MCL (Zhang et al, J. Med. Chem. 2012, 55, 8757). Alternatively, MCL derivatives have been prepared via modification of the hydroxyl group in C4 via etherification or esterification (Ma W W et al, Molecules 2013, 18, 5980-5992). However, none of these modifications were found to lead to MCL analogs with improved anticancer activity.

Micheliolide (1, MCL)

Thus, there is a need in the art for new Micheliolide deriviatives and active Micheliolide deriviatives for use as anticancer and anti-inflammatory agents. The present invention fulfills this unmet need.

3. BRIEF DESCRIPTION OF THE DRAWINGS

The present invention is described herein with reference to the accompanying drawings, in which similar reference characters denote similar elements throughout the several views. It is to be understood that in some instances, various aspects of the invention may be shown exaggerated, enlarged, exploded, or incomplete to facilitate an understanding of the invention.

FIG. 1 , comprising FIG. 1A through FIG. 1C depicts P450-mediated oxyfunctionalization of MCL. FIG. 1A depicts the synthesis of oxyfunctionalized MCL derivatives via oxidation of micheliolide (1) with engineered P450 variant FL #62. Products: 2(R)-hydroxy-micheliolide (2), 14-hydroxy-micheliolide (3), 14-CHO-micheliolide (4). FIG. 1B depicts the large scale synthesis of 2(R)-hydroxy-(2) and 14-hydroxy-MCL (3) using engineered P450 variants V-F10 and V-H10. FIG. 1C depicts the large scale synthesis of 14-hydroxy-MCL (3) using engineered P450 variant V-H10.

FIG. 2 depicts the synthesis and chemical structures of C2-substituted derivatives of micheliolide prepared according to the methods provided herein.

FIG. 3 depicts the synthesis and chemical structures of C14-substituted derivatives of micheliolide prepared according to the methods provided herein.

FIG. 4 depicts the synthesis and chemical structure of C2,C4-disubstituted and C4,C14-disubstituted micheliolide derivatives prepared according to the methods provided herein.

FIG. 5 depicts the chemical structures of C2-substituted derivatives of micheliolide prepared according to the methods provided herein.

FIG. 6 depicts the chemical structures of C14-substituted derivatives of micheliolide prepared according to the methods provided herein.

FIG. 7 depicts the synthesis of C2,C13-disubstituted and C13,C14-disubstituted micheliolide derivatives according to the methods provided herein.

FIG. 8 depicts the antileukemic activity of MCL and MCL derivatives as measured based on reduction of cell viability of AML cells (M9-ENL1) upon incubation with the compound at 20 μM.

FIG. 9 depicts the antileukemic activity of MCL and MCL derivatives as measured based on cytotoxicity ((LD₅₀) against AML cells (M9-ENL1).

FIG. 10 depicts the antileukemic activity of MCL and MCL derivatives as measured based on cytotoxicity (LD₅₀) against four different primary human acute myelogenous leukemia (AML) specimens.

FIG. 11 depicts the cytotoxicity of MCL and MCL derivatives against prostate cancer cells (PC-3) as measured based on reduction of cell viability upon incubation with the compound at 20 μM.

FIG. 12 depicts the cytotoxicity of MCL and MCL derivatives against brain cancer cells (U343MG) as measured based on reduction of cell viability upon incubation with the compound at 20 μM.

FIG. 13 depicts the cytotoxicity of MCL and MCL derivatives against neuroblastoma cells (SK-N-MC) as measured based on reduction of cell viability upon incubation with the compound at 20 μM.

FIG. 14 depicts the cytotoxicity of MCL and MCL derivatives against lung cancer cells (A549) as measured based on reduction of cell viability upon incubation with the compound at 20 μM.

FIG. 15 depicts the cytotoxicity of MCL and MCL derivatives against skin cancer cells (SK-MEL-2) as measured based on reduction of cell viability upon incubation with the compound at 20 μM.

FIG. 16 depicts the cytotoxicity of MCL and MCL derivatives against cervical cancer cells (HeLa) as measured based on reduction of cell viability upon incubation with the compound at 20 μM.

4. DETAILED DESCRIPTION OF THE INVENTION

Methods are provided for the generation of novel micheliolide derivatives functionalized at carbon atoms C2 and C14. The invention is based on the discovery that engineered variants of cytochrome P450 enzymes can be used to carry out the hydroxylation of these sites in micheliolide. According to the methods disclosed herein, these P450-catalyzed C—H hydroxylation reactions can be coupled to chemical interconversion of the enzymatically introduced hydroxyl group in order to install a broad range of functionalities at these otherwise unreactive sites of the molecule. As further demonstrated herein, the methods provided herein can also be applied to enable the production of bifunctionalized micheliolide derivatives, which in addition to modifications at the level of carbon atom C2 or C14, are also functionalized at the level of carbon atom C13.

While currently available methods have permitted the preparation of C13-modified MCL derivatives, the methods provided herein enable the modification of additional positions in the MCL scaffold. These methods can be useful to functionalize the C2 and C14 positions, optionally in conjunction with functionalization at the C13 position, to generate next-generation micheliolide derivatives with unexpectedly improved pharmacological properties.

Prior to this disclosure, the utility of cytochrome P450 enzymes and engineered variants thereof, for MCL oxyfunctionalization was unknown. The inventors discovered that engineered variants of natural cytochrome P450 monooxygenase enzymes can be exploited for the purpose of hydroxylating aliphatic positions in the MCL carbocyclic backbone (i.e. position C2 and C14) with high efficiency (i.e. high turnover numbers) and, in some cases, with excellent degrees of regio- and stereoselectivity, while preserving the integrity of critical functionalities in the molecule, such as the α-methylene-γ-lactone moiety and the 4,5-epoxide group.

The synthesis of C2- or C14-functionalized derivatives of micheliolide has never been described before. The present invention provides methods to generate derivatives of this type via a two-step chemoenzymatic strategy, in which micheliolide is first hydroxylated to generate 2-hydroxy-micheliolide or 14-hydroxy-micheliolide by means of one or more P450 monooxygenase enzyme(s). These hydroxylated derivatives can be isolated (e.g., via chromatography or extraction) and then subjected to chemical reaction conditions suitable for converting the enzymatically installed hydroxyl group (—OH) into a different functional group, such as, for example, a halogen, an ether group, a thioether group, an acyloxy group, an amide group, or an amino group. Several reagents and reaction conditions are known in the art to perform the chemical interconversion of a hydroxyl group (—OH), including reagents and reaction conditions for alkylation, acylation, deoxohalogenation, and nucleophilic substitution of an hydroxyl group (—OH).

Furthermore, using the methods provided herein it is also possible to first generate 2- or 14-substituted micheliolide derivatives chemoenzymatically and then use these compounds as intermediates to synthesize doubly substituted micheliolide derivatives (i.e. C2,C13-disubstituted derivatives, C14,C13-disubstituted derivatives), in which the C13 position is also modified. Within this aspect of the invention, previously reported methods that are suitable for the functionalization of the C13 site in parthenolide (Guzman, Rossi et al. 2006; Hwang, Chang et al. 2006; Nasim and Crooks 2008; Han, Barrios et al. 2009; Neelakantan, Nasim et al. 2009; Woods, Mo et al. 2011) (See also Crooks et. al, U.S. Pat. Nos. 7,312,242; 7,678,904; 8,124,652) can be applied, as long as the reaction conditions involved in these processes are compatible with the functional group(s) contained within the substituent preinstalled in position C2 or C14.

For clarity of disclosure, and not by way of limitation, the detailed description of the invention is divided into the subsections set forth below.

4.1 Definitions

The term “functional group” as used herein refers to a contiguous group of atoms that, together, may undergo a chemical reaction under certain reaction conditions. Examples of functional groups are, among many others, —OH, —NH₂, —SH, —(C═O)—, —N₃, —C≡CH.

The term “aliphatic” or “aliphatic group” as used herein means a straight or branched C₁₋₁₅ hydrocarbon chain that is completely saturated or that contains one or more units of unsaturation, or a monocyclic C₃₋₈ hydrocarbon, or bicyclic C₈₋₁₂ hydrocarbon that is completely saturated or that contains one or more units of unsaturation, but which is not aromatic (also referred to herein as “cycloalkyl”). For example, suitable aliphatic groups include, but are not limited to, linear or branched alkyl, alkenyl, alkynyl groups or hybrids thereof such as (cycloalkyl)alkyl, (cycloalkenyl)alkyl, or (cycloalkynyl)alkyl. The alkyl, alkenyl, or alkynyl group may be linear, branched, or cyclic and may contain up to 15, preferably up to 8, and most preferably up to 5 carbon atoms. Preferred alkyl groups include methyl, ethyl, propyl, cyclopropyl, butyl, cyclobutyl, pentyl, and cyclopentyl groups. Preferred alkenyl groups include propenyl, butenyl, and pentenyl groups. Preferred alkynyl groups include propynyl, butynyl, and pentynyl groups.

The term “aryl” and “aryl group” as used herein refers to an aromatic substituent containing a single aromatic or multiple aromatic rings that are fused together, directly linked, or indirectly linked (such as linked through a methylene or an ethylene moiety). A aryl group may contain from 5 to 24 carbon atoms, preferably 5 to 18 carbon atoms, and most preferably 5 to 14 carbon atoms.

The terms “heteroatom” means nitrogen, oxygen, or sulphur, and includes any oxidized forms of nitrogen and sulfur, and the quaternized form of any basic nitrogen. Heteroatom further include Se, Si, and P.

The term “heteroaryl” as used herein refer to an aryl group in which at least one carbon atom is replaced with a heteroatom. Preferably, a heteroaryl group is a 5- to 18-membered, particularly a 5- to 14-membered, and especially a 5- to 10-membered aromatic ring system containing at least one heteroatom selected from the group consisting of oxygen, sulphur, and nitrogen atoms. Preferred heteroaryl groups include pyridyl, pyrrolyl, furyl, thienyl, indolyl, isoindolyl, indolizinyl, imidazolyl, pyridonyl, pyrimidyl, pyrazinyl, oxazolyl, thiazolyl, purinyl, quinolinyl, isoquinolinyl, benzofuranyl, and benzoxazolyl groups.

A heterocyclic group may be any monocyclic or polycyclic ring system which contains at least one heteroatom and may be unsaturated or partially or fully saturated. The term “heterocyclic” thus includes heteroaryl groups as defined above as well as non-aromatic heterocyclic groups. Preferably, a heterocyclic group is a 3- to 18-membered, particularly a 3- to 14-membered, and especially a 3- to 10-membered, ring system containing at least one heteroatom selected from the group consisting of oxygen, sulphur, and nitrogen atoms. Preferred heterocyclic groups include the specific heteroaryl groups listed above as well as pyranyl, piperidinyl, pyrrolidinyl, dioaxanyl, piperazinyl, morpholinyl, thiomorpholinyl, morpholinosulfonyl, tetrahydroisoquinolinyl, and tetrahydrofuranyl groups.

A halogen atom may be a fluorine, chlorine, bromine, or iodine atom.

By “optionally substituted”, it is intended that in the any of the chemical groups listed above (e.g., alkyl, alkenyl, alkynyl, heteroalkyl, heteroalkenyl, heteroalkynyl, aryl, heteroaryl, heterocyclic, triazolyl groups), one or more hydrogen atoms are optionally replaced with an atom or chemical group other than hydrogen. Specific examples of such substituents include, without limitation, halogen atoms, hydroxyl (—OH), sulfhydryl (—SH), substituted sulfhydryl, carbonyl (—CO—), carboxy (—COOH), amino (—NH₂), nitro (—NO₂), sulfo (—SO₂—OH), cyano (—CN), thiocyanato (—S—C≡N), phosphono (—P(O)OH₂), alkyl, alkenyl, alkynyl, heteroalkyl, heteroalkenyl, heteroalkynyl, aryl, heteroaryl, heterocyclic, alkylthiol, alkyloxy, alkylamino, arylthiol, aryloxy, or arylamino groups. Where “optionally substituted” modifies a series of groups separated by commas (e.g., “optionally substituted A, B, or C”; or “A, B, or C optionally substituted with”), it is intended that each of the groups (e.g., A, B, or C) is optionally substituted.

The term “contact” as used herein with reference to interactions of chemical units indicates that the chemical units are at a distance that allows short range non-covalent interactions (such as Van der Waals forces, hydrogen bonding, hydrophobic interactions, electrostatic interactions, dipole-dipole interactions) to dominate the interaction of the chemical units. For example, when a protein is ‘contacted’ with a chemical species, the protein is allowed to interact with the chemical species so that a reaction between the protein and the chemical species can occur.

The term “polypeptide”, “protein”, and “enzyme” as used herein refers to any chain of two or more amino acids bonded in sequence, regardless of length or post-translational modification. According to their common use in the art, the term “protein” refers to any polypeptide consisting of more than 50 amino acid residues. These definitions are however not intended to be limiting.

In general, the term “mutant” or “variant” as used herein with reference to a molecule such as polynucleotide or polypeptide, indicates that such molecule has been mutated from the molecule as it exists in nature. In particular, the term “mutate” and “mutation” as used herein indicates any modification of a nucleic acid and/or polypeptide which results in an altered nucleic acid or polypeptide. Mutations include any process or mechanism resulting in a mutant protein, enzyme, polynucleotide, or gene. A mutation can occur in a polynucleotide or gene sequence, by point mutations, deletions, or insertions of single or multiple nucleotide residues. A mutation in a polynucleotide includes mutations arising within a protein-encoding region of a gene as well as mutations in regions outside of a protein-encoding sequence, such as, but not limited to, regulatory or promoter sequences. A mutation in a coding polynucleotide such as a gene can be “silent”, i.e., not reflected in an amino acid alteration upon expression, leading to a “sequence-conservative” variant of the gene. A mutation in a polypeptide includes but is not limited to mutation in the polypeptide sequence and mutation resulting in a modified amino acid. Non-limiting examples of a modified amino acid include a glycosylated amino acid, a sulfated amino acid, a prenylated (e.g., famesylated, geranylgeranylated) amino acid, an acetylated amino acid, an acylated amino acid, a PEGylated amino acid, a biotinylated amino acid, a carboxylated amino acid, a phosphorylated amino acid, and the like.

The term “engineer” or “engineered” refers to any manipulation of a molecule that result in a detectable change in the molecule, wherein the manipulation includes but is not limited to inserting a polynucleotide and/or polypeptide heterologous to the cell and mutating a polynucleotide and/or polypeptide native to the cell.

The term “polynucleotide molecule” as used herein refers to any chain of two or more nucleotides bonded in sequence. For example, a nucleic acid molecule can be a DNA or a RNA.

The terms “vector” and “vector construct” as used herein refer to a vehicle by which a DNA or RNA sequence (e.g., a foreign gene) can be introduced into a host cell, so as to transform the host and promote expression (e.g., transcription and translation) of the introduced sequence. A common type of vector is a “plasmid”, which generally is a self-contained molecule of double-stranded DNA that can be readily accept additional (foreign) DNA and which can be readily introduced into a suitable host cell. A large number of vectors, including plasmid and fungal vectors, have been described for replication and/or expression in a variety of eukaryotic and prokaryotic hosts. Non-limiting examples include pKK plasmids (Clonetech), pUC plasmids, pET plasmids (Novagen, Inc., Madison, Wis.), pRSET or pREP plasmids (Invitrogen, San Diego, Calif.), or pMAL plasmids (New England Biolabs, Beverly, Mass.), and many appropriate host cells, using methods disclosed or cited herein or otherwise known to those skilled in the relevant art. The terms “express” and “expression” refer to allowing or causing the information in a gene or DNA sequence to become manifest, for example producing a protein by activating the cellular functions involved in transcription and translation of a corresponding gene or DNA sequence. A DNA sequence is expressed in or by a cell to form an “expression product” such as a protein. The expression product itself, e.g., the resulting protein, may also be the to be “expressed” by the cell. A polynucleotide or polypeptide is expressed recombinantly, for example, when it is expressed or produced in a foreign host cell under the control of a foreign or native promoter, or in a native host cell under the control of a foreign promoter.

The term “fused” as used herein means being connected through one or more covalent bonds. The term “bound” as used herein means being connected through non-covalent interactions. Examples of non-covalent interactions are van der Waals, hydrogen bond, electrostatic, and hydrophobic interactions. The term “tethered” as used herein means being connected through covalent or non-covalent interactions. Thus, a “polypeptide tethered to a solid support” refers to a polypeptide that is connected to a solid support (e.g., surface, resin bead) either via non-covalent interactions or through covalent bonds.

4.2 P450 Monooxygenase Enzymes

The present invention provides cytochrome P450 polypeptides having the capability to oxidize micheliolide, wherein the cytochrome P450 polypeptide comprises an amino acid sequence having at least 90% sequence identity to CYP102A1 from Bacillus megaterium (SEQ ID NO: 1) or to the CYP102A1 variant FL #62 (SEQ. ID NO:2).

In one embodiment, the P450 polypeptide comprises an amino acid sequence having at least 90% sequence identity to CYP102A1 from Bacillus megaterium. In one embodiment, the CYP102A1 from Bacillus megaterium comprises an amino acid sequence of:

(SEQ ID NO: 1) MTIKEMPQPKTFGELKNLPLLNTDKPVQALMKIADELGEIFKFEAPGRV TRYLSSQRLIKEACDESRFDKNLSQALKFVRDFAGDGLFTSWTHEKNWK KAHNILLPSFSQQAMKGYHAMMVDIAVQLVQKWERLNADEHIEVPEDMT RLTLDTIGLCGFNYRFNSFYRDQPHPFITSMVRALDEAMNKLQRANPDD PAYDENKRQFQEDIKVMNDLVDKIIADRKASGEQSDDLLTHMLNGKDPE TGEPLDDENIRYQIITFLIAGHETTSGLLSFALYFLVKNPHVLQKAAEE AARVLVDPVPSYKQVKQLKYVGMVLNEALRLWPTAPAFSLYAKEDTVLG GEYPLEKGDELMVLIPQLHRDKTIWGDDVEEFRPERFENPSAIPQHAFK PFGNGQRACIGQQFALHEATLVLGMMLKHFDFEDHTNYELDIKETLTLK PEGFVVKAKSKKIPLGGIPSPSTEQSAKKVRKKAENAHNTPLLVLYGSN MGTAEGTARDLADIAMSKGFAPQVATLDSHAGNLPREGAVLIVTASYNG HPPDNAKQFVDWLDQASADEVKGVRYSVFGCGDKNWATTYQKVPAFIDE TLAAKGAENIADRGEADASDDFEGTYEEWREHMWSDVAAYFNLDIENSE DNKSTLSLQFVDSAADMPLAKMHGAFSTNVVASKELQQPGSARSTRHLE IELPKEASYQEGDHLGVIPRNYEGIVNRVTARFGLDASQQIRLEAEEEK LAHLPLAKTVSVEELLQYVELQDPVTRTQLRAMAAKTVCPPHKVELEAL LEKQAYKEQVLAKRLTMLELLEKYPACEMKFSEFIALLPSIRPRYYSIS SSPRVDEKQASITVSVVSGEAWSGYGEYKGIASNYLAELQEGDTITCFI STPQSEFTLPKDPETPLIMVGPGTGVAPFRGFVQARKQLKEQGQSLGEA HLYFGCRSPHEDYLYQEELENAQSEGIITLHTAFSRMPNQPKTYVQHVM EQDGKKLIELLDQGAHFYICGDGSQMAPAVEATLMKSYADVHQVSEADA RLWLQQLEEKGRYAKDVWAG

In one embodiment, the P450 polypeptide comprises an amino acid sequence having at least 90% sequence identity to CYP102A1 variant FL #62 from Bacillus megaterium. In one embodiment, the CYP102A1 variant FL #62 from Bacillus megaterium comprises an amino acid sequence of:

(SEQ ID NO: 2) MTIKEMPQPKTFGELKNLPLLNTDKPVQALMKIADELGEIFKFEAPGRV TRYLSSQRLIKEACDESRFDKNLSQALKFARDSVGDGLATSWTHEKNWK KAHNILLPSFSQQAMKGYHAMMVDIAVQLVQKWERLNADEHIEVSEDMT RLTLDTIGLCGFNYRFNSFYRDQPHPFIISMVRTLDEVMNKLQRANPDD PVYDENKRQCQEDIKVMNDLVDKIIADRKARGEQSDDLLTQMLNGKDPE TGEPLDDGNISYQIITFLIAGHETTSGLLSFALYFLVKNPHVLQKVAEE AARVLVDPVPSYKQVKQLKYVGMVLNEALRLWPTAPAFSLYAKEDTVLG GEYPLEKGDEVMVLIPQLHRDKTIWGDDVEEFRPERFENPSAIPQHAFK PFGNGQRACIGQQFALHEATLVLGMMLKHFDFEDHTNYELDIKETLTLK PEGFVVKAKSKKIPLGGIPSPSTEQSAKKVRKKAENAHNTPLLVLYGSN MGTAEGTARDLADIAMSKGFAPQVATLDSHAGNLPREGAVLIVTASYNG HPPDNAKQFVDWLDQASADEVKGVRYSVFGCGDKNWATTYQKVPAFIDE TLAAKGAENIADRGEADASDDFEGTYEEWREHMWSDVAAYFNLDIENSE DNKSTLSLQFVDSAADMPLAKMHGAFSTNVVASKELQQPGSARSTRHLE IELPKEASYQEGDHLGVIPRNYEGIVNRVTARFGLDASQQIRLEAEEEK LAHLPLAKTVSVEELLQYVELQDPVTRTQLRAMAAKTVCPPHKVELEAL LEKQAYKEQVLAKRLTMLELLEKYPACEMKFSEFIALLPSIRPRYYSIS SSPRVDEKQASITVSVVSGEAWSGYGEYKGIASNYLAELQEGDTITCFI STPQSEFTLPKDPETPLIMVGPGTGVAPFRGFVQARKQLKEQGQSLGEA HLYFGCRSPHEDYLYQEELENAQSEGIITLHTAFSRMPNQPKTYVQHVM EQDGKKLIELLDQGAHFYICGDGSQMAPAVEATLMKSYADVHQVSEADA RLWLQQLEEKGRYAKDVWAG.

In one embodiment, the P450 polypeptide comprises an amino acid sequence having at least 90% sequence identity to CYP102A1 variant FL #46 from Bacillus megaterium. In one embodiment, the CYP102A1 variant FL #46 from Bacillus megaterium comprises an amino acid sequence of:

(SEQ ID NO: 3) MTIKEMPQPKTFGELKNLPLLNTDKPVQALMKIADELGEIFKFEAPGCV TRYLSSQRLIKEACDESRFDKNLSQALKAVRDFAGDGLITSWTHEINWK KAHNILLPSFSQQAMKGYHAMMVDIAVQLVQKWERLNADEHIEVSEDMT RLTLDTIGLCGFNYRFNSFYRDQPHPFIISMVRALDEVMNKLQRANPDD PAYDENKRQCQEDIKVMNDLVDKIIADRKARGEQSDDLLTQMLNGKDPE TGEPLDDGNISYQIITFLIAGHETTSGLLSFALYFLVKNPHVLQKVAEE AARVLVDPVPSYKQVKQLKYVGMVLNEALRLWPTAPAFSLYAKEDTVLG GEYPLEKGDEVMVLIPQLHRDKTIWGDDVEEFRPERFENPSAIPQHAFK PFGNGQRACIGQQFALHEATLVLGMMLKHFDFEDHTNYELDIKETLTLK PEGFVVKAKSKKIPLGGIPSPSTEQSAKKVRKKAENAHNTPLLVLYGSN MGTAEGTARDLADIAMSKGFAPQVATLDSHAGNLPREGAVLIVTASYNG HPPDNAKQFVDWLDQASADEVKGVRYSVFGCGDKNWATTYQKVPAFIDE TLAAKGAENIADRGEADASDDFEGTYEEWREHMWSDVAAYFNLDIENSE DNKSTLSLQFVDSAADMPLAKMHGAFSTNVVASKELQQPGSARSTRHLE IELPKEASYQEGDHLGVIPRNYEGIVNRVTARFGLDASQQIRLEAEEEK LAHLPLAKTVSVEELLQYVELQDPVTRTQLRAMAAKTVCPPHKVELEAL LEKQAYKEQVLAKRLTMLELLEKYPACEMKFSEFIALLPSIRPRYYSIS SSPRVDEKQASITVSVVSGEAWSGYGEYKGIASNYLAELQEGDTITCFI STPQSEFTLPKDPETPLIMVGPGTGVAPFRGFVQARKQLKEQGQSLGEA HLYFGCRSPHEDYLYQEELENAQSEGIITLHTAFSRMPNQPKTYVQHVM EQDGKKLIELLDQGAHFYICGDGSQMAPAVEATLMKSYADVHQVSEADA RLWLQQLEEKGRYAKDVWAG.

In one embodiment, the P450 polypeptide comprises an amino acid sequence having at least 90% sequence identity to CYP102A1 variant FL #47 from Bacillus megaterium. In one embodiment, the CYP102A1 variant FL #47 from Bacillus megaterium comprises an amino acid sequence of:

(SEQ ID NO: 4) MTIKEMPQPKTFGELKNLPLLNTDKPVQALMKIADELGEIFKFEAPGCV TRYLSSQRLIKEACDESRFDKNLSQALKAVRDFAGDGLATSWTHEINWK KAHNILLPSFSQQAMKGYHAMMVDIAVQLVQKWERLNADEHIEVSEDMT RLTLDTIGLCGFNYRFNSFYRDQPHPFIISMVRALDEVMNKLQRANPDD PAYDENKRQCQEDIKVMNDLVDKIIADRKARGEQSDDLLTQMLNGKDPE TGEPLDDGNISYQIITFLIAGHETTSGLLSFALYFLVKNPHVLQKVAEE AARVLVDPVPSYKQVKQLKYVGMVLNEALRLWPTAPAFSLYAKEDTVLG GEYPLEKGDEVMVLIPQLHRDKTIWGDDVEEFRPERFENPSAIPQHAFK PFGNGQRACIGQQFALHEATLVLGMMLKHFDFEDHTNYELDIKETLTLK PEGFVVKAKSKKIPLGGIPSPSTEQSAKKVRKKAENAHNTPLLVLYGSN MGTAEGTARDLADIAMSKGFAPQVATLDSHAGNLPREGAVLIVTASYNG HPPDNAKQFVDWLDQASADEVKGVRYSVFGCGDKNWATTYQKVPAFIDE TLAAKGAENIADRGEADASDDFEGTYEEWREHMWSDVAAYFNLDIENSE DNKSTLSLQFVDSAADMPLAKMHGAFSTNVVASKELQQPGSARSTRHLE IELPKEASYQEGDHLGVIPRNYEGIVNRVTARFGLDASQQIRLEAEEEK LAHLPLAKTVSVEELLQYVELQDPVTRTQLRAMAAKTVCPPHKVELEAL LEKQAYKEQVLAKRLTMLELLEKYPACEMKFSEFIALLPSIRPRYYSIS SSPRVDEKQASITVSVVSGEAWSGYGEYKGIASNYLAELQEGDTITCFI STPQSEFTLPKDPETPLIMVGPGTGVAPFRGFVQARKQLKEQGQSLGEA HLYFGCRSPHEDYLYQEELENAQSEGIITLHTAFSRMPNQPKTYVQHVM EQDGKKLIELLDQGAHFYICGDGSQMAPAVEATLMKSYADVHQVSEADA RLWLQQLEEKGRYAKDVWAG.

In one embodiment, the P450 polypeptide comprises an amino acid sequence having at least 90% sequence identity to CYP102A1 variant V-F10 from Bacillus megaterium. In one embodiment, the CYP102A1 variant V-F10 from Bacillus megaterium comprises an amino acid sequence of:

(SEQ ID NO: 5) MTIKEMPQPKTFGELKNLPLLNTDKPVQALMKIADELGEIFKFEAPGRV TRYLSSQRLIKEACDESRFDKNLSQALKFARAAVGDGLATSWTHEKNWK KAHNILLPSFSQQAMKGYHAMMVDIAVQLVQKWERLNADEHIEVSEDMT RLTLDTIGLCGFNYRFNSFYRDQPHPFIISMVRTLDEVMNKLQRANPDD PVYDENKRQCQEDIKVMNDLVDKIIADRKARGEQSDDLLTQMLNGKDPE TGEPLDDGNISYQIITFLIAGHETTSGLLSFALYFLVKNPHVLQKVAEE AARVLVDPVPSYKQVKQLKYVGMVLNEALRLWPTAPAFSLYAKEDTVLG GEYPLEKGDEVMVLIPQLHRDKTIWGDDVEEFRPERFENPSAIPQHAFK PFGNGQRACIGQQFALHEATLVLGMMLKHFDFEDHTNYELDIKETLTLK PEGFVVKAKSKKIPLGGIPSPSTEQSAKKVRKKAENAHNTPLLVLYGSN MGTAEGTARDLADIAMSKGFAPQVATLDSHAGNLPREGAVLIVTASYNG HPPDNAKQFVDWLDQASADEVKGVRYSVFGCGDKNWATTYQKVPAFIDE TLAAKGAENIADRGEADASDDFEGTYEEWREHMWSDVAAYFNLDIENSE DNKSTLSLQFVDSAADMPLAKMHGAFSTNVVASKELQQPGSARSTRHLE IELPKEASYQEGDHLGVIPRNYEGIVNRVTARFGLDASQQIRLEAEEEK LAHLPLAKTVSVEELLQYVELQDPVTRTQLRAMAAKTVCPPHKVELEAL LEKQAYKEQVLAKRLTMLELLEKYPACEMKFSEFIALLPSIRPRYYSIS SSPRVDEKQASITVSVVSGEAWSGYGEYKGIASNYLAELQEGDTITCFI STPQSEFTLPKDPETPLIMVGPGTGVAPFRGFVQARKQLKEQGQSLGEA HLYFGCRSPHEDYLYQEELENAQSEGIITLHTAFSRMPNQPKTYVQHVM EQDGKKLIELLDQGAHFYICGDGSQMAPAVEATLMKSYADVHQVSEADA RLWLQQLEEKGRYAKDVWAG

In one embodiment, the P450 polypeptide comprises an amino acid sequence having at least 90% sequence identity to CYP102A1 variant V-H10 from Bacillus megaterium. In one embodiment, the CYP102A1 variant V-H10 from Bacillus megaterium comprises an amino acid sequence of:

(SEQ ID NO: 6) MTIKEMPQPKTFGELKNLPLLNTDKPVQALMKIADELGEIFKFEAPGRV TRYLSSQRLIKEACDESRFDKNLSQALKNARFAVGDGLATSWTHEKNWK KAHNILLPSFSQQAMKGYHAMMVDIAVQLVQKWERLNADEHIEVSEDMT RLTLDTIGLCGFNYRFNSFYRDQPHPFIISMVRTLDEVMNKLQRANPDD PVYDENKRQCQEDIKVMNDLVDKIIADRKARGEQSDDLLTQMLNGKDPE TGEPLDDGNISYQIITFLIAGHETTSGLLSFALYFLVKNPHVLQKVAEE AARVLVDPVPSYKQVKQLKYVGMVLNEALRLWPTAPAFSLYAKEDTVLG GEYPLEKGDEVMVLIPQLHRDKTIWGDDVEEFRPERFENPSAIPQHAFK PFGNGQRACIGQQFALHEATLVLGMMLKHFDFEDHTNYELDIKETLTLK PEGFVVKAKSKKIPLGGIPSPSTEQSAKKVRKKAENAHNTPLLVLYGSN MGTAEGTARDLADIAMSKGFAPQVATLDSHAGNLPREGAVLIVTASYNG HPPDNAKQFVDWLDQASADEVKGVRYSVFGCGDKNWATTYQKVPAFIDE TLAAKGAENIADRGEADASDDFEGTYEEWREHMWSDVAAYFNLDIENSE DNKSTLSLQFVDSAADMPLAKMHGAFSTNVVASKELQQPGSARSTRHLE IELPKEASYQEGDHLGVIPRNYEGIVNRVTARFGLDASQQIRLEAEEEK LAHLPLAKTVSVEELLQYVELQDPVTRTQLRAMAAKTVCPPHKVELEAL LEKQAYKEQVLAKRLTMLELLEKYPACEMKFSEFIALLPSIRPRYYSIS SSPRVDEKQASITVSVVSGEAWSGYGEYKGIASNYLAELQEGDTITCFI STPQSEFTLPKDPETPLIMVGPGTGVAPFRGFVQARKQLKEQGQSLGEA HLYFGCRSPHEDYLYQEELENAQSEGIITLHTAFSRMPNQPKTYVQHVM EQDGKKLIELLDQGAHFYICGDGSQMAPAVEATLMKSYADVHQVSEADA RLWLQQLEEKGRYAKDVWAG

In one embodiment, the P450 polypeptide comprises an amino acid sequence having at least 90% sequence identity to CYP102A1 variant VIII-B1 from Bacillus megaterium. In one embodiment, the CYP102A1 variant VIII-B1 from Bacillus megaterium comprises an amino acid sequence of:

(SEQ ID NO: 7) MTIKEMPQPKTFGELKNLPLLNTDKPVQALMKIADELGEIFKFEAPGRV TRYLSSQRLIKEACDESRFDKNLSTALKNARFSVGDGFATSWTHEKNWK KAHNILLPSFSQQAMKGYHAMMVDIAVQLVQKWERLNADEHIEVSEDMT RLTLDTIGLCGFNYRFNSFYRDQPHPFIISMVATLDEVMNKLQRANPDD PVYDENKRQCQEDIKVMNDLVDKIIADRKARGEQSDDLLTQMLNGKDPE TGEPLDDGNISYQIITFLIAGHETTSGLLSFALYFLVKNPHVLQKVAEE AARVLVDPVPSYKQVKQLKYVGMVLNEALRLWPTAPAFSLYAKEDTVLG GEYPLEKGDEVMVLIPQLHRDKTIWGDDVEEFRPERFENPSAIPQHAFK PFGNGQRACIGQQFALHEATLVLGMMLKHFDFEDHTNYELDIKETLTLK PEGFVVKAKSKKIPLGGIPSPSTEQSAKKVRKKAENAHNTPLLVLYGSN MGTAEGTARDLADIAMSKGFAPQVATLDSHAGNLPREGAVLIVTASYNG HPPDNAKQFVDWLDQASADEVKGVRYSVFGCGDKNWATTYQKVPAFIDE TLAAKGAENIADRGEADASDDFEGTYEEWREHMWSDVAAYFNLDIENSE DNKSTLSLQFVDSAADMPLAKMHGAFSTNVVASKELQQPGSARSTRHLE IELPKEASYQEGDHLGVIPRNYEGIVNRVTARFGLDASQQIRLEAEEEK LAHLPLAKTVSVEELLQYVELQDPVTRTQLRAMAAKTVCPPHKVELEAL LEKQAYKEQVLAKRLTMLELLEKYPACEMKFSEFIALLPSIRPRYYSIS SSPRVDEKQASITVSVVSGEAWSGYGEYKGIASNYLAELQEGDTITCFI STPQSEFTLPKDPETPLIMVGPGTGVAPFRGFVQARKQLKEQGQSLGEA HLYFGCRSPHEDYLYQEELENAQSEGIITLHTAFSRMPNQPKTYVQHVM EQDGKKLIELLDQGAHFYICGDGSQMAPAVEATLMKSYADVHQVSEADA RLWLQQLEEKGRYAKDVWAG

In some embodiments, the capability to oxidize micheliolide corresponds to the capability of the cytochrome P450 polypeptide to hydroxylate a C—H bond attached to the carbon atom C2 in micheliolide, where the resulting hydroxylated product has predominantly (S) or (R) stereochemistry at the hydroxylation site (C2) according to the stereoselectivity of the enzyme. In other embodiments, such capability corresponds to the capability of the cytochrome P450 polypeptide to hydroxylate a C—H bond attached to the carbon atom C14 in micheliolide.

Cytochrome P450 polypeptides are provided that are capable of hydroxylating a C—H bond at position 2, position 14, or both, in micheliolide, and which have an improved property compared with a reference enzyme, such as the naturally occurring enzymes from which they were derived, the naturally occurring enzymes being CYP102A1 from Bacillus megaterium (SEQ ID NO: 1).

In the characterization of the cytochrome P450 enzymes disclosed herein, the polypeptides can be described in reference to the amino acid sequence of a naturally occurring cytochrome P450 enzyme or another engineered cytochrome P450 enzyme. As such, the amino acid residue is determined in the cytochrome P450 enzymes beginning from the initiating methionine (M) residue (i.e., M represent residue position 1), although it will be understood that this initiating methionine residue may be removed by biological processing machinery such as in a host cell or in vitro translation system, to generate a mature protein lacking the initiating methionine residue. The amino acid residue position at which a particular amino acid or amino acid change is present is sometimes described herein as “Xn”, or “position n”, where n refers to the residue position.

As described above, the cytochrome P450 enzymes provided herein are characterized by an improved enzyme property as compared to the naturally occurring parent enzyme or another engineered cytochrome P450 enzyme. Changes to enzyme properties can include, among others, improvements in enzymatic activity, regioselectivity, stereoselectivity, and/or reduced substrate or product inhibition. In one embodiment, the altered properties are based on engineered cytochrome P450 polypeptides having residue differences at specific residue positions as compared to a reference sequence of a naturally occurring cytochrome P450 enzyme, such as CYP102A1 (SEQ ID NO: 1).

In some embodiments, the P450 monoxygenase is an engineered variant of CYP102A1 (SEQ ID NO: 1). In one embodiment, the variant of SEQ ID NO:1 comprises an amino acid change at one or more of the following positions of SEQ ID NO: 1: X26, X27, X43, X48, X52, X53, X73, X75, X76, X79, X82, X83, X88, X89, X95, X97, X143, X146, X176, X181, X182, X185, X189, X198, X206, X226, X227, X237, X253, X256, X261, X264, X265, X268, X269, X291, X320, X331, X329, X330, X354, X355, X367, X394, X435, X436, X444, X446, X438, and X439.

In some embodiments, the cytochrome P450 polypeptides can have additionally one or more residue differences at residue positions not specified by an X above as compared to the sequence SEQ ID NO: 1 or SEQ ID NO: 2. In some embodiments, the differences can be 1-2, 1-5, 1-10, 1-20, 1-30, 1-40, 1-50, 1-75, 1-100, 1-150, or 1-200 residue differences at other amino acid residue positions not defined by X above.

In some embodiments, the cytochrome P450 polypeptides can have additionally one or more residue differences at residue positions not specified by an X above and located within the “heme domain” of the enzyme, as compared to the sequence SEQ ID NO: 1 or SEQ ID NO: 2. In some embodiments, the differences can be 1-2, 1-5, 1-10, 1-20, 1-30, 1-40, 1-50, 1-75, 1-100, 1-150, or 1-200 residue differences at other amino acid residue positions not defined by X above and located within the “heme domain” of the enzyme.

In some embodiments, the engineered cytochrome P450 polypeptides having one or more of the improved enzyme properties described herein, can comprise an amino acid sequence that is at least 60%, 70%, 80%, 85%, 90%, 95%, 99% or more identical to the sequence SEQ ID NO: 1 or SEQ ID NO: 2.

In some embodiments, the engineered cytochrome P450 polypeptides having one or more of the improved enzyme properties described herein, can comprise an amino acid sequence encompassing its heme domain which is at least 60%, 70%, 80%, 85%, 90%, 95%, 99% or more identical to the amino acid sequence encompassing the first 500 amino acids in the sequence SEQ ID NO: 1 or SEQ ID NO: 2 (i.e. residue 1 to residue 500 in these reference sequences).

In some embodiments, the improved cytochrome P450 polypeptide can comprise an amino acid sequence that is at least 90% or more identical to a sequence corresponding to one of SEQ ID NOS: 2, 3, 4, 5, 6, and 7.

In some embodiments, the improved cytochrome P450 polypeptide can comprise an amino acid sequence encompassing its heme domain that is at least 90% or more identical to the sequence encompassing the first 500 amino acids in one of SEQ ID NOS: 2, 3, 4, 5, 6, and 7.

In some embodiments, the improved cytochrome P450 polypeptide comprises an amino acid sequence corresponding to the sequence of one of SEQ ID NOS: 2, 3, 4, 5, 6, and 7.

The capability of the engineered cytochrome P450 polypeptides to oxidize micheliolide, also referred to herein as “substrate,” can be established according to methods well known in the art. Most typically, such capability can be established by contacting the substrate with the P450 monooxygenase under suitable reaction conditions in which the P450 monooxygenase is catalytically functional, and then determining the formation of an oxidized product of the substrate (e.g., hydroxylated product) by standard analytical methods such as, for example, thin-layer chromatography, HPLC, and/or LC-MS.

Various art-known methods can be applied for measuring the catalytic activity of the engineered cytochrome P450 polypeptide on parthenolide, also referred to herein as “substrate activity”. Such substrate activity can be measured by measuring the decrease of the amount of substrate, the accumulation of an oxygenation product derived from the substrate (e.g., hydroxylated product), or the accumulation of an oxidation byproduct generated during the enzymatic reaction (e.g., H₂O₂), after a given time after contacting the substrate with the P450 monooxygenase under suitable reaction conditions in which the P450 monooxygenase is catalytically functional. Other methods to measure the substrate activity include measuring the consumption of a cofactor (e.g., NADPH or NADH) or cosubstrate (O₂) utilized by the enzyme during the oxidation reaction. The choice of the method will vary depending on the specific application such as, for example, according to the nature of the substrate, the nature of the monooxygenase (e.g., its NAD(P)H cofactor specificity), and the number of the P450 monooxygenases that are to be evaluated. A person skilled in the art will be capable of selecting the most appropriate method in each case.

The substrate activity of engineered cytochrome P450 polypeptides can be measured and expressed in terms of number of catalytic turnovers, product formation rate, cofactor consumption rate, O₂ consumption rate, H₂O₂ consumption rate (e.g., for H₂O₂-dependent monooxygenases), and the like. Most conveniently, such substrate activity can be measured and expressed in terms of total turnover numbers (or TTN), which corresponds to the total number of catalytic turnovers supported by the P450 monooxygenase enzyme on this substrate.

In some embodiments, the engineered cytochrome P450 polypeptides disclosed herein are capable of supporting at least 1, 10, 50, 100, or more TTN in the oxidation of micheliolide.

The regio- and stereoselectivity of the engineered cytochrome P450 polypeptides for the oxidation of micheliolide can be measured by determining the relative distribution of oxidation products generated by the reaction between the substrate and the cytochrome P450 polypeptide using conventional analytical methods such as, for example, (chiral) normal phase liquid chromatography, (chiral) reverse-phase liquid chromatography, or (chiral) gas chromatography. In some instances, the oxidation products can be subjected to a chemical derivatization process to facilitate these analyses. For example, the hydroxylation products obtained from the reaction of the P450 polypeptide with micheliolide can be derivatized using an UV-active acid chloride (e.g., benzoyl chloride) prior to separation and quantification by HPLC.

In some embodiments, the engineered cytochrome P450 polypeptides disclosed herein are capable of hydroxylating a C—H bond connected to the C2 or C14 carbon atom in micheliolide with a regioselectivity of 1%, 5%, 10%, 25%, 50%, 75%, 90%, 95%, or higher.

In some embodiments, the polypeptide described herein can be provided in form of a kit. These kits may contain an individual enzyme or a plurality of enzymes. The kits can further include reagents for carrying out the enzymatic reactions, substrates for assessing the activity of the enzymes, and reagents for detecting the products. The kits can also include instructions for the use of the kits.

In some embodiments, the polypeptides described herein can be covalently or non-covalently linked to a solid support for the purpose, for example, of screening the enzymes for activity on a range of different substrates or for facilitating the separation of reactants and products from the enzyme after the enzymatic reactions. Examples of solid supports include but are not limited to, organic polymers such as polystyrene, polyacrylamide, polyethylene, polypropylene, polyethyleneglycole, and the like, and inorganic materials such as glass, silica, controlled pore glass, metals. The configuration of the solid support can be in the form of beads, spheres, particles, gel, a membrane, or a surface.

4.3 Polynucleotides and Host Cells for Expression of P450 Monooxygenase Enzymes

In another aspect, the present invention provides polynucleotide molecules encoding for the improved cytochrome P450 polypeptides disclosed herein. The polynucleotides may be linked to one or more regulatory sequences controlling the expression of the cytochrome P450 polypeptide-encoding gene to form a recombinant polynucleotide capable of expressing the polypeptide.

Since the correspondence of all the possible three-base codons to the various amino acids is known, providing the amino acid sequence of the P450 polypeptide provides also a description of all the polynucleotide molecules encoding for such polypeptide. Thus, a person skilled in the art will be able, given a certain polypeptide sequence, to generate any number of different polynucleotides encoding for the same polypeptide. Preferably, the codons are selected to fit the host cell in which the polypeptide is being expressed. For example, preferred codons used in bacteria are preferably used to express the polypeptide in a bacterial host.

In some embodiments, the polynucleotide molecule comprises a nucleotide sequence encoding for a cytochrome P450 polypeptide with an amino acid sequence that is at least 60%, 70%, 80%, 85%, 90%, 95%, 99% or more identical to SEQ ID NO: 1, 2, 3, 4 5, 6 or 7.

In some embodiments, the polynucleotide molecule encoding for the improved cytochrome P450 polypeptide is comprised in a recombinant expression vector. Examples of suitable recombinant expression vectors include but are not limited to, chromosomal, nonchromosomal and synthetic DNA sequences, e.g., derivatives of SV40; bacterial plasmids; phage DNA; baculovirus; yeast plasmids; vectors derived from combinations of plasmids and phage DNA, viral DNA such as vaccinia, adenovirus, fowl pox virus, pseudorabies, adenovirus, adeno-associated viruses, retroviruses and many others. Any vector that transduces genetic material into a cell, and, if replication is desired, which is replicable and viable in the relevant host can be used. A large number of expression vectors and expression hosts are known in the art, and many of these are commercially available. A person skilled in the art will be able to select suitable expression vectors for a particular application, e.g., the type of expression host (e.g., in vitro systems, prokaryotic cells such as bacterial cells, and eukaryotic cells such as yeast, insect, or mammalian cells) and the expression conditions selected.

In another aspect, the present invention provides an expression host system comprising a polynucleotide molecule encoding for the improved cytochrome P450 polypeptides disclosed herein. Expression host systems that may be used within the invention include any systems that support the transcription, translation, and/or replication of a polynucleotide molecule provided herein. Preferably, the expression host system is a cell. Host cells for use in expressing the polypeptides encoded by the expression vector disclosed herein are well known in the art and include but are not limited to, bacterial cells (e.g., Escherichia coli, Streptomyces); fungal cells such as yeast cells (e.g., Saccharomyces cerevisiae, Pichia pastoris); insect cells; plant cells; and animal cells. The expression host systems also include lysates of prokaryotic cells (e.g., bacterial cells) and lysates of eukaryotic cells (e.g., yeast, insect, or mammalian cells). These systems also include in vitro transcription/translation systems, many of which are commercially available. The choice of the expression vector and host system depends on the type of application intended for the methods provided herein and a person skilled in the art will be able to select a suitable expression host based on known features and application of the different expression hosts.

4.4 Methods of Preparing and Using the Engineered Cytochrome P450 Polypeptides

The engineered cytochrome P450 polypeptides can be prepared via mutagenesis of the polynucleotide encoding for the naturally occurring cytochrome P450 enzymes (SEQ ID NO: 1, 2, or 3) or for an engineered variant thereof. Many mutagenesis methods are known in the art and these include, but are not limited to, site-directed mutagenesis, site-saturation mutagenesis, random mutagenesis, cassette-mutagenesis, DNA shuffling, homologous recombination, non-homologous recombination, site-directed recombination, and the like. Detailed description of art-known mutagenesis methods can be found, among other sources, in U.S. Pat. Nos. 5,605,793; 5,830,721; 5,834,252; WO 95/22625; WO 96/33207; WO 97/20078; WO 97/35966; WO 98/27230; WO 98/42832; WO 99/29902; WO 98/41653; WO 98/41622; WO 98/42727; WO 00/18906; WO 00/04190; WO 00/42561; WO 00/42560; WO 01/23401; WO 01/64864.

Numerous methods for making nucleic acids encoding for polypeptides having a predetermined or randomized sequence are known to those skilled in the art. For example, oligonucleotide primers having a predetermined or randomized sequence can be prepared chemically by solid phase synthesis using commercially available equipments and reagents. Polynucleotide molecules can then be synthesized and amplified using a polymerase chain reaction, digested via endonucleases, ligated together, and cloned into a vector according to standard molecular biology protocols known in the art (e.g., Sambrook et al. Molecular Cloning: A Laboratory Manual (Third Edition), Cold Spring Harbor Press, 2001). These methods, in combination with the mutagenesis methods mentioned above, can be used to generate polynucleotide molecules that encode for engineered cytochrome P450 polypeptides as well as suitable vectors for the expression of these polypeptides in a host expression system.

Engineered cytochrome P450 polypeptides expressed in a host expression system, such as, for example, in a host cell, can be isolated and purified using any one or more of the well-known techniques for protein purification, including, among others, cell lysis via sonication or chemical treatment, filtration, salting-out, and chromatography (e.g., ion-exchange chromatography, gel-filtration chromatography, etc.).

The recombinant P450 polypeptides obtained from mutagenesis of a parental P450 enzyme sequences (e.g., one of SEQ ID NO: 1-7 or engineered variants thereof) can be screened for identifying engineered P450 polypeptides having improved enzyme properties, such as improvements with respect to their catalytic activity, coupling efficiency, regioselectivity and/or stereoselectivity for the oxidation of parthenolide. The improvement resulting from the introduced amino acid mutation(s) in any one or more of these enzyme properties can be then measured according to methods known in the art, as described above.

In some embodiments, a method is provided for oxidizing micheliolide, the method comprising

-   -   a. contacting micheliolide with an engineered cytochrome P450         polypeptide;     -   b. allowing for the engineered cytochrome P450 enzyme to         catalyze the hydroxylation of a C—H bond within micheliolide,         while preserving α-methylene-γ-lactone moiety therein, thereby         producing a hydroxylated micheliolide derivative;     -   c. isolating the hydroxylated micheliolide derivative.

In some embodiments, the C—H bond hydroxylated by the engineered cytochrome P450 polypeptide within the method is attached to carbon C14 in micheliolide.

In some embodiments, the C—H bond hydroxylated by the engineered cytochrome P450 polypeptide within the method is attached to carbon C2 in micheliolide. In this case, and in some embodiment, either the 2(S)- or the 2(R)-hydroxy product is produced in stereomeric excess.

In some embodiments, the engineered cytochrome P450 polypeptide used in the method comprises an amino acid sequence that is at least 60%, 70%, 80%, 85%, 90%, 95%, 99% or more identical to the sequence of one of SEQ ID NO: 1-7.

In some embodiments, the amino acid sequence encompassing the heme domain of the engineered cytochrome P450 polypeptide used in the method comprises has an amino acid sequence that is at least 60%, 70%, 80%, 85%, 90%, 95%, 99% or more identical to the amino acid sequence encompassing the first 500 amino acids in the sequences of one of SEQ ID NO: 1-7 (i.e. residue 1 to residue 500 in these sequences).

As it is known in the art, P450-catalyzed reactions typically require a source of oxygen (as co-substrate) as well as a source of reducing equivalents (i.e., electrons) to drive catalysis. Most typically, and in preferred embodiments, oxygen is provided in the form of molecular oxygen. The source of reducing equivalents can be provided in the form of a soluble cofactor, and in most preferred embodiments, it is provided in the form of reduced nicotinamide adenine dinucleotide phosphate (NADPH), which is the cofactor utilized by the cytochrome P450 enzymes disclosed herein, namely the polypeptides with one of SEQ ID NO: 1-7, and engineered variants thereof, as described above.

Alternative sources of reducing equivalents include but are not limited to, reduced nicotinamide adenine dinucleotide (NADH) or an electrode. Alternatively, chemical compounds that can serve as source of both oxygen and electrons such as for example, hydrogen peroxide (H₂O₂) or organic peroxides may also be used.

In some embodiments, the P450 reactions are carried out in the presence of a NADPH cofactor regeneration system or a NADH cofactor regeneration system. Suitable NADPH regeneration systems include but are not limited to, those based on glucoses-6-phosphate dehydrogenase or on NADP⁺-utilizing phosphite dehydrogenase variants. (van der Donk and Zhao 2003; Zhao and van der Donk 2003) Suitable NADH regeneration systems include but are not limited to, those based on glucose dehydrogenase, phosphite dehydrogenase, or formate dehydrogenase (van der Donk and Zhao 2003; Zhao and van der Donk 2003).

Typically, the P450 reactions are carried out in a buffered aqueous solution. Various buffering agents such as phosphate, acetate, TRIS, MOPS, HEPES, etc. can be used. An organic cosolvent such as, for example, methanol, ethanol, dimethylsulfoxide, dimethylformamide, etc. can be added, provided these cosolvent and their relative concentration in the cosolvent system does not completely inactivate the P450 enzyme.

In carrying out the P450 reactions described herein, the engineered P450 enzymes may be added to the reaction mixture in the form of purified enzymes, whole cells containing the P450 enzymes, and/or cell extracts and/or lysates of such cells.

Typically, the P450 reactions are allowed to proceed until a substantial amount of the substrate is transformed into the product. Product formation (or substrate consumption) can be monitored using standard analytical methods such as, for example, thin-layer chromatography, GC, HPLC, or LC-MS. Experimental parameters such as amount of P450 enzyme added to the reaction mixture, temperature, solvent composition, cofactor concentration, composition of the cofactor regeneration system, etc. can be readily optimized by routine experimentation and a person skilled in the art will be able to identify most suitable reaction conditions according to the substrate and the P450 enzyme utilized in the process.

4.5 Micheliolide Derivatives

The engineered P450 polypeptides provided herein provide a means for introducing a hydroxyl group (—OH) in aliphatic positions of the carbocyclic backbone of micheliolide, such as position C2 or position C14, whose chemical functionalization have never been accomplished before. According to the methods provided herein, the enzymatically installed hydroxyl group can be converted into a variety of other functional groups through versatile methods for chemical hydroxyl group interconversion, such as nucleophilic substitution (e.g., Mitsunobu substitution), alkylation, acylation, deoxyhalogenation, O—H carbene insertion, and the like.

Accordingly, micheliolide derivatives are provided that are modified at the level of carbon atom C2 or C14, or double-modified at the level of carbon atom C2 and C4, or C4 and C14. Furthermore, micheliolide derivatives are provided that are (doubly) functionalized at the level of carbon atoms C2 and C13 or at the level of carbon atoms C14 and C13. Notably, some of these compounds were found to possess significantly improved anticancer activity compared to MCL, while others combined improved anticancer activity with increased water solubility as compared to MCL.

A compound of general formula (A) or a salt thereof is provided:

-   -   wherein     -   A is ═CH₂ or —CH₂R* wherein R* is an amino acid residue bonded         to the A methylene via a nitrogen or sulfur atom; or R* is         —NR¹R², —NR¹C(O)R², —NR¹CO₂R², or —SR¹, wherein R¹ and R² are         independently selected from the group consisting of H and an         optionally substituted alkyl, alkenyl, or alkynyl group, an         optionally substituted heteroalkyl, heteroalkenyl, or         heteroalkynyl group, an optionally substituted aryl group, an         optionally substituted heteroaryl group, or an optionally         substituted heterocyclic group; or R* is —NR¹R², wherein R¹ and         R² optionally together with the nitrogen atom form a an         optionally substituted 5-12 membered ring, the ring optionally         comprising at least one heteroatom or group selected from the         group consisting of —CO—, —SO—, —SO₂—, and —PO—;     -   L is —O—, —NH—, —NHC(O)—, —OC(O)—, —OC(O)NH—, —S—, —SO—, —SO₂—,         —PO—, —OCH₂—, or a chemical bond connecting the carbon atom to         Y; and Y represents a hydrogen atom, an optionally substituted         alkyl, alkenyl, or alkynyl group, an optionally substituted         heteroalkyl, heteroalkenyl, or heteroalkynyl group, an         optionally substituted aryl group, an optionally substituted         heteroaryl group, or an optionally substituted heterocyclic         group, with the proviso that when -L-Y is hydrogen, -M-X is not         hydroxyl, nor —C(O)CH₂CH₃ and A is not —CH₂—N(CH₃)₂, wherein         -L-Y together with the carbon atom at position C2 optionally         forms carbonyl; or     -   Y is absent and L represents a halogen atom, an azido group         (—N₃), an optionally substituted triazole group, or a group         —NR³R⁴, where R³ represents a hydrogen atom or an optionally         substituted alkyl, alkenyl, or alkynyl group; R⁴ represents an         optionally substituted alkyl, alkenyl, alkynyl, aryl, or         heteroaryl group; or where R³ and R⁴ are connected together to         form an optionally substituted heterocyclic group;     -   M is —O— or —OC(O)— and X represents a hydrogen atom, an         optionally substituted alkyl, alkenyl, or alkynyl group, an         optionally substituted heteroalkyl, heteroalkenyl, or         heteroalkynyl group, an optionally substituted aryl group, an         optionally substituted heteroaryl group, or an optionally         substituted heterocyclic group.

In some embodiments, the present invention provides compounds of formula (A), wherein wherein L is —OC(O)—; Y is hydrogen, —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, —(C₁-C₆) alkyl, —CH₂—(C₆-C₁₀) aryl, or —NH—(C₆-C₁₀) aryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂, or CH₂R*, where R* is selected from the group consisting of methylamino (—NH(CH₃)), dimethylamino (—N(CH₃)₂), methylethylamino (—N(CH₃)(CH₂CH₃)), methylpropylamino (—N(CH₃)(CH₂CH₂CH₃)), methylisopropylamino (—(CH₃)(CH₂(CH₃)₂), (—N(CH₃)(CH₂CH₂OH), pyrrolidine, piperidine, 4-methylpiperidine, 1-phenylmethanamine (—NCH₂Ph), and 2-phenylethanamine (—NCH₂CHPh); M is —O—, or —OC(O)—; X is hydrogen, —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, (C₁-C₆) alkyl, —N(CH₃)₂—(C₆-C₁₀) aryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen. Preferably, L is —OC(O)—; Y is —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, or —NH—(C₆-C₁₀) aryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, halogen, phenyl, and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂; M is —O—, or —OC(O)—; X is hydrogen, —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen.

In some embodiments, the present invention provides compounds of formula (A), wherein L is —O—; Y is —C(O)—(C₆-C₁₀) aryl, —C(O)—-(5-14 membered) heteroaryl, hydrogen, —CH₂—(C₆-C₁₀) aryl, —C(O)—NH—(C₆-C₁₀) aryl, or —(C₁-C₆) alkyl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂, or CH₂R*, where R* is selected from the group consisting of methylamino (—NH(CH₃)), dimethylamino (—N(CH₃)₂), methylethylamino (—N(CH₃)(CH₂CH₃)), methylpropylamino (—N(CH₃)(CH₂CH₂CH₃)), methylisopropylamino (—(CH₃)(CH₂(CH₃)₂), (—N(CH₃)(CH₂CH₂OH), pyrrolidine, piperidine, 4-methylpiperidine, 1-phenylmethanamine (—NCH₂Ph), and 2-phenylethanamine (—NCH₂CHPh); M is —O—, or —OC(O)—; X is hydrogen, —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, (C₁-C₆) alkyl, —N(CH₃)₂—(C₆-C₁₀) aryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen. Preferably, L is —O—; Y is —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, or —NH—(C₆-C₁₀) aryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, halogen, phenyl, and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂; M is —O—, or —OC(O)—; X is hydrogen, —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen.

In some embodiments, the present invention provides compounds of formula (A), wherein -L-Y is hydrogen, hydroxyl, azide, -(5-14 membered) heteroaryl, amino, halogen, —NH—C(O)—(C₆-C₁₀) aryl, wherein -(5-14 membered) heteroaryl is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂; M is —O—; X is hydrogen, or —C(O)—(C₆-C₁₀) aryl, wherein —C(O)—(C₆-C₁₀) aryl is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen. Preferably, -L-Y is hydrogen, hydroxyl, -(5-14 membered) heteroaryl, halogen, wherein -(5-14 membered) heteroaryl is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂; X is hydrogen, or —C(O)—(C₆-C₁₀) aryl, wherein —C(O)—(C₆-C₁₀) aryl is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen.

A compound of general formula (B) or a slat thereof is provided:

-   -   wherein     -   A is ═CH₂ or —CH₂R* wherein R* is an amino acid residue bonded         to the A methylene via a nitrogen or sulfur atom; or R* is         —NR¹R², —NR¹C(O)R², —NR¹CO₂R², or —SR¹, wherein R¹ and R² are         independently selected from the group consisting of H and an         optionally substituted alkyl, alkenyl, or alkynyl group, an         optionally substituted heteroalkyl, heteroalkenyl, or         heteroalkynyl group, an optionally substituted aryl group, an         optionally substituted heteroaryl group, or an optionally         substituted heterocyclic group; or R* is —NR¹R², wherein R¹ and         R² optionally together with the nitrogen atom form a an         optionally substituted 5-12 membered ring, the ring optionally         comprising at least one heteroatom or group selected from the         group consisting of —CO—, —SO—, —SO₂—, and —PO—;     -   L is —O—, —NH—, —NHC(O)—, —OC(O)—, —OC(O)NH—, —S—, —SO—, —SO₂—,         —PO—, —OCH₂—, or a chemical bond connecting the carbon atom to         Y; and Y represents a hydrogen atom, an optionally substituted         alkyl, alkenyl, or alkynyl group, an optionally substituted         heteroalkyl, heteroalkenyl, or heteroalkynyl group, an         optionally substituted aryl group, an optionally substituted         heteroaryl group, or an optionally substituted heterocyclic         group, with the proviso that when -L-Y is hydrogen, -M-X is not         hydroxyl, nor —C(O)CH₂CH₃ and A is not —CH₂—N(CH₃)₂, wherein         -L-Y together with the carbon atom at position C2 optionally         forms carbonyl; or     -   Y is absent and L represents a halogen atom, an azido group         (—N₃), an optionally substituted triazole group, or a group         —NR³R⁴, where R³ represents a hydrogen atom or an optionally         substituted alkyl, alkenyl, or alkynyl group; R⁴ represents an         optionally substituted alkyl, alkenyl, alkynyl, aryl, or         heteroaryl group; or where R³ and R⁴ are connected together to         form an optionally substituted heterocyclic group;     -   M is —O— or —OC(O)— and X represents a hydrogen atom, an         optionally substituted alkyl, alkenyl, or alkynyl group, an         optionally substituted heteroalkyl, heteroalkenyl, or         heteroalkynyl group, an optionally substituted aryl group, an         optionally substituted heteroaryl group, or an optionally         substituted heterocyclic group.

In some embodiments, the present invention provides compounds of formula (B), wherein wherein L is —OC(O)—; Y is hydrogen, —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, —(C₁-C₆) alkyl, —CH₂—(C₆-C₁₀) aryl, or —NH—(C₆-C₁₀) aryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂, or CH₂R*, where R* is selected from the group consisting of methylamino (—NH(CH₃)), dimethylamino (—N(CH₃)₂), methylethylamino (—N(CH₃)(CH₂CH₃)), methylpropylamino (—N(CH₃)(CH₂CH₂CH₃)), methylisopropylamino (—(CH₃)(CH₂(CH₃)₂), (—N(CH₃)(CH₂CH₂OH), pyrrolidine, piperidine, 4-methylpiperidine, 1-phenylmethanamine (—NCH₂Ph), and 2-phenylethanamine (—NCH₂CHPh); M is —O—, or —OC(O)—; X is hydrogen, —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, (C₁-C₆) alkyl, —N(CH₃)₂—(C₆-C₁₀) aryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen. Preferably, L is —OC(O)—; Y is —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, or —NH—(C₆-C₁₀) aryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, halogen, phenyl, and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂; M is —O—, or —OC(O)—; X is hydrogen, —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen.

In some embodiments, the present invention provides compounds of formula (B), wherein L is —O—; Y is —C(O)—(C₆-C₁₀) aryl, —C(O)— -(5-14 membered) heteroaryl, hydrogen, —CH₂—(C₆-C₁₀) aryl, —C(O)—NH—(C₆-C₁₀) aryl, or —(C₁-C₆) alkyl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂, or CH₂R*, where R* is selected from the group consisting of methylamino (—NH(CH₃)), dimethylamino (—N(CH₃)₂), methylethylamino (—N(CH₃)(CH₂CH₃)), methylpropylamino (—N(CH₃)(CH₂CH₂CH₃)), methylisopropylamino (—(CH₃)(CH₂(CH₃)₂), (—N(CH₃)(CH₂CH₂OH), pyrrolidine, piperidine, 4-methylpiperidine, 1-phenylmethanamine (—NCH₂Ph), and 2-phenylethanamine (—NCH₂CHPh); M is —O—, or —OC(O)—; X is hydrogen, —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, (C₁-C₆) alkyl, —N(CH₃)₂—(C₆-C₁₀) aryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen. Preferably, L is —O—; Y is —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, or —NH—(C₆-C₁₀) aryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, halogen, phenyl, and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂; M is —O—, or —OC(O)—; X is hydrogen, —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen.

In some embodiments, the present invention provides compounds of formula (B), wherein -L-Y is hydrogen, hydroxyl, azide, -(5-14 membered) heteroaryl, amino, halogen, —NH—C(O)—(C₆-C₁₀) aryl, wherein -(5-14 membered) heteroaryl is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂; M is —O—; X is hydrogen, or —C(O)—(C₆-C₁₀) aryl, wherein —C(O)—(C₆-C₁₀) aryl is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen. Preferably, -L-Y is hydrogen, hydroxyl, -(5-14 membered) heteroaryl, halogen, wherein -(5-14 membered) heteroaryl is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂; X is hydrogen, or —C(O)—(C₆-C₁₀) aryl, wherein —C(O)—(C₆-C₁₀) aryl is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen.

A compound of general formula (I) or salt thereof is provided:

-   -   wherein     -   L represents —O—, —NH—, —NHC(O)—, —OC(O)—, —OC(O)NH—, —S—, —SO—,         —SO₂—, —PO—, —OCH₂—, or a chemical bond connecting the carbon         atom to Y; and Y represents a hydrogen atom, an optionally         substituted alkyl, alkenyl, or alkynyl group, an optionally         substituted heteroalkyl, heteroalkenyl, or heteroalkynyl group,         an optionally substituted aryl group, an optionally substituted         heteroaryl group, or an optionally substituted heterocyclic         group; or Y is absent and L represents a halogen atom, an azido         group (—N₃), an optionally substituted triazole group, or L         represents a group —NR³R⁴, where R³ represents a hydrogen atom         or an optionally substituted alkyl, alkenyl, or alkynyl group;         R⁴ represents an optionally substituted alkyl, alkenyl, alkynyl,         aryl, or heteroaryl group; or where R³ and R⁴ are connected         together to form an optionally substituted heterocyclic group.

A compound of general formula (II) or salt thereof is also provided:

-   -   wherein     -   L represents —O—, —NH—, —NHC(O)—, —OC(O)—, —OC(O)NH—, —S—, —SO—,         —SO₂—, —PO—, —OCH₂—, or a chemical bond connecting the carbon         atom to Y; and Y represents a hydrogen atom, an optionally         substituted alkyl, alkenyl, or alkynyl group, an optionally         substituted heteroalkyl, heteroalkenyl, or heteroalkynyl group,         an optionally substituted aryl group, an optionally substituted         heteroaryl group, or an optionally substituted heterocyclic         group; or Y is absent and L represents a halogen atom, an azido         group (—N₃), an optionally substituted triazole group, or L         represents a group —NR³R⁴, where R³ represents a hydrogen atom         or an optionally substituted alkyl, alkenyl, or alkynyl group;         R⁴ represents an optionally substituted alkyl, alkenyl, alkynyl,         aryl, or heteroaryl group; or where R³ and R⁴ are connected         together to form an optionally substituted heterocyclic group.

A compound of general formula (III) or salt thereof is also provided:

-   -   wherein     -   L represents —O—, —NH—, —NHC(O)—, —OC(O)—, —OC(O)NH—, —S—, —SO—,         —O₂—, —PO—, —OCH₂—, or a chemical bond connecting the carbon         atom to Y; and Y represents a hydrogen atom, an optionally         substituted alkyl, alkenyl, or alkynyl group, an optionally         substituted heteroalkyl, heteroalkenyl, or heteroalkynyl group,         an optionally substituted aryl group, an optionally substituted         heteroaryl group, or an optionally substituted heterocyclic         group; or Y is absent and L represents a halogen atom, an azido         group (—N₃), an optionally substituted triazole group, or L         represents a group —NR³R⁴, where R³ represents a hydrogen atom         or an optionally substituted alkyl, alkenyl, or alkynyl group;         R⁴ represents an optionally substituted alkyl, alkenyl, alkynyl,         aryl, or heteroaryl group; or where R³ and R⁴ are connected         together to form an optionally substituted heterocyclic group;         and     -   M represents —O—, —NH—, —NHC(O)—, —OC(O)—, —OC(O)NH—, —S—, —SO—,         —O₂—, —PO—, —OCH₂—, or a chemical bond connecting the carbon         atom to X; and X represents a hydrogen atom, an optionally         substituted alkyl, alkenyl, or alkynyl group, an optionally         substituted heteroalkyl, heteroalkenyl, or heteroalkynyl group,         an optionally substituted aryl group, an optionally substituted         heteroaryl group, or an optionally substituted heterocyclic         group; or X is absent and M represents a halogen atom, an azido         group (—N₃), an optionally substituted triazole group, or M         represents a group —NR³R⁴, where R³ represents a hydrogen atom         or an optionally substituted alkyl, alkenyl, or alkynyl group;         R⁴ represents an optionally substituted alkyl, alkenyl, alkynyl,         aryl, or heteroaryl group; or where R³ and R⁴ are connected         together to form an optionally substituted heterocyclic group.

A compound of general formula (IV) or salt thereof is also provided:

-   -   wherein     -   L represents —O—, —NH—, —NHC(O)—, —OC(O)—, —OC(O)NH—, —S—, —SO—,         —O₂—, —PO—, —OCH₂—, or a chemical bond connecting the carbon         atom to Y; and Y represents a hydrogen atom, an optionally         substituted alkyl, alkenyl, or alkynyl group, an optionally         substituted heteroalkyl, heteroalkenyl, or heteroalkynyl group,         an optionally substituted aryl group, an optionally substituted         heteroaryl group, or an optionally substituted heterocyclic         group; or Y is absent and L represents a halogen atom, an azido         group (—N₃), an optionally substituted triazole group, or L         represents a group —NR³R⁴, where R³ represents a hydrogen atom         or an optionally substituted alkyl, alkenyl, or alkynyl group;         R⁴ represents an optionally substituted alkyl, alkenyl, alkynyl,         aryl, or heteroaryl group; or where R³ and R⁴ are connected         together to form an optionally substituted heterocyclic group;         and     -   M represents —O—, —NH—, —NHC(O)—, —OC(O)—, —OC(O)NH—, —S—, —SO—,         —O₂—, —PO—, —OCH₂—, or a chemical bond connecting the carbon         atom to X; and X represents a hydrogen atom, an optionally         substituted alkyl, alkenyl, or alkynyl group, an optionally         substituted heteroalkyl, heteroalkenyl, or heteroalkynyl group,         an optionally substituted aryl group, an optionally substituted         heteroaryl group, or an optionally substituted heterocyclic         group; or X is absent and M represents a halogen atom, an azido         group (—N₃), an optionally substituted triazole group, or M         represents a group —NR³R⁴, where R³ represents a hydrogen atom         or an optionally substituted alkyl, alkenyl, or alkynyl group;         R⁴ represents an optionally substituted alkyl, alkenyl, alkynyl,         aryl, or heteroaryl group; or where R³ and R⁴ are connected         together to form an optionally substituted heterocyclic group.

A compound of general formula (V) or salt thereof is also provided:

-   -   wherein     -   A is —CH₂R* wherein R* is an amino acid residue bonded to the A         methylene via a nitrogen or sulfur atom; or R* is —NR¹R²,         —NR¹C(O)R², —NR¹CO₂R², or —SR¹, wherein R¹ and R² are         independently selected from the group consisting of H and an         optionally substituted alkyl, alkenyl, or alkynyl group, an         optionally substituted heteroalkyl, heteroalkenyl, or         heteroalkynyl group, an optionally substituted aryl group, an         optionally substituted heteroaryl group, and an optionally         substituted heterocyclic group; or where R* is —NR¹R², R¹ and R²         optionally together with the nitrogen atom form a an optionally         substituted 5-12 membered ring, the ring optionally comprising         one or more heteroatoms or a group selected from the group         consisting of —CO—, —SO—, —SO₂—, and —PO—;     -   L represents —O—, —NH—, —NHC(O)—, —OC(O)—, —OC(O)NH—, —S—, —SO—,         —SO₂—, —PO—, —OCH₂—, or a chemical bond connecting the carbon         atom to Y;     -   Y represents a hydrogen atom, an optionally substituted alkyl,         alkenyl, or alkynyl group, an optionally substituted         heteroalkyl, heteroalkenyl, or heteroalkynyl group, an         optionally substituted aryl group, an optionally substituted         heteroaryl group, or an optionally substituted heterocyclic         group;     -   or Y is absent and L represents a halogen atom, an azido group         (—N₃), an optionally substituted triazole group, or L represents         a group —NR³R⁴, where R³ represents a hydrogen atom or an         optionally substituted alkyl, alkenyl, or alkynyl group; R⁴         represents an optionally substituted alkyl, alkenyl, alkynyl,         aryl, or heteroaryl group; or where R³ and R⁴ are connected         together to form an optionally substituted heterocyclic group.

A compound of general formula (VI) or salt thereof is also provided:

-   -   wherein,     -   A is —CH₂R* wherein R* is an amino acid residue bonded to the A         methylene via a nitrogen or sulfur atom; or R* is —NR¹R²,         —NR¹C(O)R², —NR¹CO₂R², or —SR¹, wherein R¹ and R² are         independently selected from the group consisting of H and an         optionally substituted alkyl, alkenyl, or alkynyl group, an         optionally substituted heteroalkyl, heteroalkenyl, or         heteroalkynyl group, an optionally substituted aryl group, an         optionally substituted heteroaryl group, and an optionally         substituted heterocyclic group; or where R* is —NR¹R², R₁ and R₂         optionally together with the nitrogen atom form a an optionally         substituted 5-12 membered ring, the ring optionally comprising         one or more heteroatoms or a group selected from the group         consisting of —CO—, —SO—, —SO₂—, and —PO—;     -   L represents —O—, —NH—, —NHC(O)—, —OC(O)—, —OC(O)NH—, —S—, —SO—,         —SO₂—, —PO—, —OCH₂—, or a chemical bond connecting the carbon         atom to Y;     -   Y represents a hydrogen atom, an optionally substituted alkyl,         alkenyl, or alkynyl group, an optionally substituted         heteroalkyl, heteroalkenyl, or heteroalkynyl group, an         optionally substituted aryl group, an optionally substituted         heteroaryl group, or an optionally substituted heterocyclic         group;     -   or Y is absent and L represents a halogen atom, an azido group         (—N₃), an optionally substituted triazole group, or L represents         a group —NR³R⁴, where R³ represents a hydrogen atom or an         optionally substituted alkyl, alkenyl, or alkynyl group; R⁴         represents an optionally substituted alkyl, alkenyl, alkynyl,         aryl, or heteroaryl group; or where R³ and R⁴ are connected         together to form an optionally substituted heterocyclic group.

Salts of the compounds provided herein can be prepared according to standard procedures well known in the art, for example, by reacting a compound containing a one or more sufficiently basic functional group with a suitable organic or mineral acid. Similarly, base addition salts can be prepared by reacting a compound containing a one or more sufficiently acid functional group with a suitable organic or mineral base. Examples of inorganic acid addition salts includes fluoride, chloride, bromide, iodide, sulfate, nitrate, bicarbonate, phosphate, and carbonate salts. Examples of organic acid addition salts include acetate, citrate, malonate, tartrate, succinate, lactate, malate, benzoate, ascorbate, α-ketoglutarate, tosylate, and methanesulfonate salts. Examples of base addition salts include lithium, sodium, potassium, calcium, and ammonium salts.

In specific embodiments, the substituent L in the compounds of general formula I and II is —OC(O)— and the substituent Y is phenyl, 4-pyridyl, (4-dimethylamino)phenyl, para-meta-, or orto-fluoro-phenyl, para-, meta-, or ortho-trifluoromethyl-phenyl, (2,4-bis-trifluoromethyl)phenyl, (3,5-bis-trifluoromethyl)phenyl, 1- or 2-naphthyl, 3-N-methyl-indolyl, 5-(4-chlorophenyl)isoxazolyl, 2-(4-bromophenyl)furanyl, 2-(2-(trifluoromethyl)phenyl)furanyl, or thiophene group.

In other specific embodiments, the substituent L in the compounds of general formula I and II is —O— and the substituent Y is (phenyl)methyl, (4-pyridyl)methyl, (4-dimethylaminophenyl)methyl, (para-, meta-, or ortho-fluoro-phenyl)methyl, (para-, meta-, or ortho-trifluoromethyl-phenyl)methyl, (2,4-bis-trifluoromethyl-phenyl)methyl, (3,5-bis-trifluoromethyl-phenyl)methyl, (naphthyl)methyl, (3-N-methyl-indolyl)methyl, (5-(4-chlorophenyl)isoxazolyl)methyl, (2-(4-bromophenyl)furanyl)methyl, (2-(2-(trifluoromethyl)phenyl)furanyl)methyl, or methyl(thiophene) group.

In other specific embodiments, the substituent L in the compounds of general formula I and II is —O— and the substituent Y is a group —CH(Ar′)COOR′, wherein Ar′ is selected from the group consisting of phenyl, 4-pyridyl, (4-dimethylamino)phenyl, para-, meta-, or ortho-fluoro-phenyl, para-, meta-, or ortho-trifluoromethyl-phenyl, (2,4-bis-trifluoromethyl)phenyl, (3,5-bis-trifluoromethyl)phenyl, 1- or 2-naphthyl, 3-N-methyl-indolyl, 5-(4-chlorophenyl)isoxazolyl, 2-(4-bromophenyl)furanyl, 2-(2-(trifluoromethyl)phenyl)furanyl, and thiophene group; and the R′ group is selected from the group consisting of methyl, ethyl, propyl, isopropyl, tert-butyl, benzyl, 2-morpholinoethyl, 2-morpholinoethyl, 2-(piperidin-1-yl)ethyl, and 2-(pyrrolidin-1-yl)ethyl group.

In specific embodiments, the substituent L in the compounds of general formula III and IV is —OC(O)—, the substituent Y is phenyl, 4-pyridyl, (4-dimethylamino)phenyl, para-, meta-, or orto-fluoro-phenyl, para-, meta-, or ortho-trifluoromethyl-phenyl, (2,4-bis-trifluoromethyl)phenyl, (3,5-bis-trifluoromethyl)phenyl, 1- or 2-naphthyl, 3-N-methyl-indolyl, 5-(4-chlorophenyl)isoxazolyl, 2-(4-bromophenyl)furanyl, 2-(2-(trifluoromethyl)phenyl)furanyl, or thiophene group, the substituent M is —OC(O)— and the substituent X is phenyl, 4-pyridyl, (4-dimethylamino)phenyl, para-, meta-, or orto-fluoro-phenyl, para-, meta-, or ortho-trifluoromethyl-phenyl, (2,4-bis-trifluoromethyl)phenyl, (3,5-bis-trifluoromethyl)phenyl, 1- or 2-naphthyl, 3-N-methyl-indolyl, 5-(4-chlorophenyl)isoxazolyl, 2-(4-bromophenyl)furanyl, 2-(2-(trifluoromethyl)phenyl)furanyl, or thiophene group.

In other specific embodiments, the substituent L in the compounds of general formula V and VI is —OC(O)—; the substituent Y is selected from the group consisting of phenyl, 4-pyridyl, (4-dimethylamino)phenyl, para-, meta-, or ortho-fluoro-phenyl, para-, meta-, or ortho-trifluoromethyl-phenyl, (2,4-bis-trifluoromethyl)phenyl, (3,5-bis-trifluoromethyl)phenyl, 1- or 2-naphthyl, 3-N-methyl-indolyl, 5-(4-chlorophenyl)isoxazolyl, 2-(4-bromophenyl)furanyl, 2-(2-(trifluoromethyl)phenyl)furanyl, and thiophene group; and the substituent A is —CH₂R*, where R* is selected from the group consisting of methylamino (—H(CH₃)), dimethylamino (—(CH₃)₂), methylethylamino (—N(CH₃)(CH₂CH₃)), methylpropylamino (—N(CH₃)(CH₂CH₂CH₃)), methylisopropylamino (—N(CH₃)(CH₂(CH₃)₂), —N(CH₃)(CH₂CH₂OH), pyrrolidine, piperidine, 4-methylpiperidine, 1-phenylmethanamine (—CH₂Ph), and 2-phenylethanamine (—NCH₂CH₂Ph).

In other specific embodiments, the substituent L in the compounds of general formula V and VI is —O—; the substituent Y is selected from the group consisting of (phenyl)methyl, (4-pyridyl)methyl, (4-dimethylaminophenyl)methyl, para-, meta-, or ortho-fluoro-phenyl)methyl, (para-, meta-, or ortho-trifluoromethyl-phenyl)methyl, (2,4-bis-trifluoromethyl-phenyl)methyl, (3,5-bis-trifluoromethyl-phenyl)methyl, (naphthyl)methyl, (3-N-methyl-indolyl)methyl, (5-(4-chlorophenyl)isoxazolyl)methyl, (2-(4-bromophenyl)furanyl)methyl, (2-(2-(trifluoromethyl)phenyl)furanyl)methyl, methyl(thiophenene) group, and a —CH(Ar′)COOR′ group, wherein Ar′ is selected from the group consisting of phenyl, 4-pyridyl, (4-dimethylamino)phenyl, para-, meta-, or ortho-fluoro-phenyl, para-, meta-, or ortho-trifluoromethyl-phenyl, (2,4-bis-trifluoromethyl)phenyl, (3,5-bis-trifluoromethyl)phenyl, 1- or 2-naphthyl, 3-N-methyl-indolyl, 5-(4-chlorophenyl)isoxazolyl, 2-(4-bromophenyl)furanyl, 2-(2-(trifluoromethyl)phenyl)furanyl, and thiophene group; and the R′ group is selected from the group consisting of methyl, ethyl, propyl, isopropyl, tert-butyl, benzyl, 2-morpholinoethyl, 2-morpholinoethyl, 2-(piperidin-1-yl)ethyl, and 2-(pyrrolidin-1-yl)ethyl group; and the substituent A is —CH₂R*, where R* is selected from the group consisting of methylamino (—NH(CH₃)), dimethylamino (—(CH₃)₂), methylethylamino (—N(CH₃)(CH₂CH₃)), methylpropylamino (—N(CH₃)(CH₂CH₂CH₃)), methylisopropylamino (—N(CH₃)(CH₂(CH₃)₂), —(CH₃)(CH₂CH₂OH), pyrrolidine, piperidine, 4-methylpiperidine, 1-phenylmethanamine (—NCH₂Ph), and 2-phenylethanamine (—NCH₂CH₂Ph).

A person skilled in the art will promptly recognize that several different chemical methods, including different chemical reagents and reaction conditions, are available for synthesizing the compounds of general formula I and II, once the hydroxylated micheliolide derivatives, i.e. 2-hydroxy-micheliolide (2) and 14-hydroxy-micheliolide (3, respectively, are made available. Accordingly, this invention focuses on the products of these transformations rather than on the specific chemical methods applied to achieve them, which of course can vary. It should be noted, however, that the examples included in this disclosure demonstrate the feasibility of applying common, art-known chemical transformations for hydroxyl group functional interconversion for the preparation of compounds of general formula I, II, III and IV. These include substitution or functionalization of the hydroxyl group in compound 2 and 3 via alkylation, methylation, acylation, nucleophilic substitution (e.g., Mitsunobu substitution), and deoxohalogenation (e.g., deoxofluorination). As described below, compounds of general formula V and VI can be obtained by further modifying the derivatives of general formula I and II, respectively, at the C13 position according to procedures known in the art.

Compounds of general formula I, II, III and IV are prepared by first subjecting micheliolide to a reaction with a suitable P450 polypeptide in order to produce 2-hydroxy-micheliolide (compound 2) or 14-hydroxy-micheliolide (compound 3). Typically, these reactions are carried out in aqueous buffer at near-neutral pH (typically, phosphate buffer, pH 8.0) with varying amount (typically, up to 20%) of an organic solvent (typically, DMSO) to facilitate dissolution of parthenolide in the buffer. Either NAPDH or, most preferably, a NADPH cofactor regeneration system is included to provide the reducing equivalents to support the P450 reaction. Typically, a NADPH cofactor regeneration system is used, which consists of phosphite dehydrogenase, NADP⁺, and sodium phosphite. The reaction temperature can be from 4 to 50 degree Celsius. The reaction time and concentration of the P450 polypeptide in the reaction mixture can vary widely, in large part depending on the stability, catalytic rate and, catalytic efficiency of the P450 enzyme. Typically, reaction times range from 1 to 48 hours, whereas the P450 catalyst concentration range from 0.1 to 10 mol %. Purification of the hydroxylation products can be achieved by a variety of techniques, such as by normal phase liquid chromatography through silica gel; reverse-phase liquid chromatography through bonded silica gel such as octadecylsilica, octylsilica and the like; and recrystallization using pure organic solvents or solvent mixtures. After isolation, the hydroxylated micheliolide derivatives provided herein (i.e. compounds 2 and 3) can be subjected to suitable chemical reagents and reaction conditions to functionalize or substitute the hydroxyl group in C2 or C14 with a different substituent. As mentioned above, a person skilled in the art will be able to readily select such reagents and reaction conditions for the purpose of preparing compounds of general formula I, II, III and IV from 2- and 14-hydroxy-micheliolide, respectively. For example, 2- and 14-ester derivatives can be prepared via acylation of 2-hydroxy-micheliolide and 14-hydroxy-micheliolide, respectively, with an acid chloride in dichloromethane in the presence of a weakly nucleophilic base (e.g., triethylamine, triisopropylamine, or pyridine). Alternatively, such ester derivatives can be prepared via reaction with a free acid in dichloromethane in presence of a coupling reagent (e.g., dicyclohexylcarbodiimide or DCC, O-(Benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate or HBTU), and weakly nucleophilic base (e.g., triethylamine, triisopropylamine, or pyridine). Optionally, coupling catalysts (e.g., 4-dimethylamino-pyridine or DMAP, 1-Hydroxybenzotriazole or HOBt) can be added to facilitate the esterification reaction.

Doubly substituted micheliolide derivatives of general formula V and VI can be prepared by further modifying the compounds of general formula I and II described above at the reactive position C13 according to procedures known in the art. Procedures that are useful for modification of position C13 in these compounds can be found, among other sources, in the following references (Guzman, Rossi et al. 2006; Hwang, Chang et al. 2006; Nasim and Crooks 2008; Han, Barrios et al. 2009; Neelakantan, Nasim et al. 2009; Woods, Mo et al. 2011). Additional procedures suitable for C13 modification are described in Crooks et. al, U.S. Pat. Nos. 7,312,242; 7,678,904; 8,124,652. Preferably, for the purpose of preparing compounds of general formula V and VI, these aforementioned procedures for C13 modification are chosen so that they do not alter or react with any of the functional groups comprised by the substituents installed in position C2 or C14 of the micheliolide derivatives of formula I or II, respectively. A person skilled in the art will be able to choose or adapt, if necessary, suitable procedures for this purpose.

4.6 Use of Micheliolide Derivatives for Treatment of Cancer and Other Diseases

The invention also provides a pharmaceutical composition comprising an effective amount of a compound of general formula (A), (B), (I), (II, (III), (IV, (V) or (VI) or a pharmaceutically acceptable salt, ester or prodrug thereof, in combination with a pharmaceutically acceptable diluent or carrier.

The invention also provides a method of inhibiting cancer cell growth and metastasis of cancer cells, comprising administering to a mammal afflicted with cancer, an amount of a compound of general formula (A), (B), (I), (II, (III), (IV, (V) or (VI), effective to inhibit the growth of the cancer cells.

The invention also provides a method comprising inhibiting cancer cell growth by contacting the cancer cell in vitro or in vivo with an amount of a compound of formula (A), (B), (I), (II, (III), (IV, (V) or (VI), effective to inhibit the growth of the cancer cell.

The invention also provides a compound of general formulae (A), (B), (I), (II, (III), (IV, (V) or (VI) for use in medical therapy (preferably for use in treating cancer, e.g., solid tumors), as well as the use of such compound for the manufacture of a medicament useful for the treatment of cancer and other diseases/disorders described herein.

In one embodiment, the invention provides a method for inhibiting cancer cell growth. In one embodiment, the method comprises administering to a mammal afflicted with cancer an amount of a compound of the invention effective to inhibit the growth of the cancer cells. In one embodiment, the method comprises contacting the cancer cell in vitro or in vivo with an amount of a compound of the invention effective to inhibit the growth of the cancer cell.

In one embodiment, invention provides a method for treating bone marrow for human bone marrow transplant treatment of leukemia in a patient. In one embodiment, the method comprises treating bone marrow with a compound of the invention prior to reintroducing bone marrow into the patient

The following are non-limiting examples of cancers that can be treated by the disclosed methods and compositions: Acute Lymphoblastic; Acute Myeloid Leukemia; Adrenocortical Carcinoma; Adrenocortical Carcinoma, Childhood; Appendix Cancer; Basal Cell Carcinoma; Bile Duct Cancer, Extrahepatic; Bladder Cancer; Bone Cancer; Osteosarcoma and Malignant Fibrous Histiocytoma; Brain Stem Glioma, Childhood; Brain Tumor, Adult; Brain Tumor, Brain Stem Glioma, Childhood; Brain Tumor, Central Nervous System Atypical Teratoid/Rhabdoid Tumor, Childhood; Central Nervous System Embryonal Tumors; Cerebellar Astrocytoma; Cerebral Astrocytotna/Malignant Glioma; Craniopharyngioma; Ependymoblastoma; Ependymoma; Medulloblastoma; Medulloepithelioma; Pineal Parenchymal Tumors of intermediate Differentiation; Supratentorial Primitive Neuroectodermal Tumors and Pineoblastoma; Visual Pathway and Hypothalamic Glioma; Brain and Spinal Cord Tumors; Breast Cancer; Bronchial Tumors; Burkitt Lymphoma; Carcinoid Tumor; Carcinoid Tumor, Gastrointestinal; Central Nervous System Atypical Teratoid/Rhabdoid Tumor; Central Nervous System Embryonal Tumors; Central Nervous System Lymphoma; Cerebellar Astrocytoma Cerebral Astrocytoma/Malignant Glioma, Childhood; Cervical Cancer; Chordoma, Childhood; Chronic Lymphocytic Leukemia; Chronic Myelogenous Leukemia; Chronic Myeloproliferative Disorders; Colon Cancer; Colorectal Cancer; Craniopharyngioma; Cutaneous T-Cell Lymphoma; Esophageal Cancer; Ewing Family of Tumors; Extragonadal Germ Cell Tumor; Extrahepatic Bile Duct Cancer; Eye Cancer, intraocular Melanoma; Eye Cancer, Retinoblastoma; Gallbladder Cancer; Gastric (Stomach) Cancer; Gastrointestinal Carcinoid Tumor; Gastrointestinal Stromal Tumor (GIST); Germ Cell Tumor, Extracranial; Germ Cell Tumor, Extragonadal; Germ Cell Tumor, Ovarian; Gestational Trophoblastic Tumor; Glioma; Glioma, Childhood Brain Stem; Glioma, Childhood Cerebral Astrocytoma; Glioma, Childhood Visual Pathway and Hypothalamic; Hairy Cell Leukemia; Head and Neck Cancer; Hepatocellular (Liver) Cancer; Histiocytosis, Langerhans Cell; Hodgkin Lymphoma; Hypopharyngeal Cancer; Hypothalamic and Visual Pathway Glioma; intraocular Melanoma; Islet Cell Tumors; Kidney (Renal Cell) Cancer; Langerhans Cell Histiocytosis; Laryngeal Cancer; Leukemia, Acute Lymphoblastic; Leukemia, Acute Myeloid; Leukemia, Chronic Lymphocytic; Leukemia, Chronic Myelogenous; Leukemia, Hairy Cell; Lip and Oral Cavity Cancer; Liver Cancer; Lung Cancer, Non-Small Cell; Lung Cancer, Small Cell; Lymphoma, AIDS-Related; Lymphoma, Burkitt; Lymphoma, Cutaneous T-Cell; Lymphoma, Hodgkin; Lymphoma, Non-Hodgkin; Lymphoma, Primary Central Nervous System; Macroglobulinemia, Waldenstrom; Malignant Fibrous Histiocvtoma of Bone and Osteosarcoma; Medulloblastoma; Melanoma; Melanoma, intraocular (Eye); Merkel Cell Carcinoma; Mesothelioma; Metastatic Squamous Neck Cancer with Occult Primary; Mouth Cancer; Multiple Endocrine Neoplasia Syndrome, (Childhood); Multiple Myeloma/Plasma Cell Neoplasm; Mycosis; Fungoides; Myelodysplastic Syndromes; Myelodysplastic/Myeloproliferative Diseases; Myelogenous Leukemia, Chronic; Myeloid Leukemia, Adult Acute; Myeloid Leukemia, Childhood Acute; Myeloma, Multiple; Myeloproliferative Disorders, Chronic; Nasal Cavity and Paranasal Sinus Cancer; Nasopharyngeal Cancer; Neuroblastoma; Non-Small Cell Lung Cancer; Oral Cancer; Oral Cavity Cancer; Oropharyngeal Cancer; Osteosarcoma and Malignant Fibrous Histiocytoma of Bone; Ovarian Cancer; Ovarian Epithelial Cancer; Ovarian Germ Cell Tumor; Ovarian Low Malignant Potential Tumor; Pancreatic Cancer; Pancreatic Cancer, Islet Cell Tumors; Papillomatosis; Parathyroid Cancer; Penile Cancer; Pharyngeal Cancer; Pheochromocytoma; Pineal Parenchymal Tumors of Intermediate Differentiation; Pineoblastoma and Supratentorial Primitive Neuroectodermal Tumors; Pituitary Tumor; Plasma Celt Neoplasm/Multiple Myeloma; Pleuropulmonary Blastoma; Primary Central Nervous System Lymphoma; Prostate Cancer; Rectal Cancer; Renal Cell (Kidney) Cancer; Renal Pelvis and Ureter, Transitional Cell Cancer; Respiratory Tract Carcinoma Involving the NUT Gene on Chromosome 15; Retinoblastoma; Rhabdomyosarcoma; Salivary Gland Cancer; Sarcoma, Ewing Family of Tumors; Sarcoma, Kaposi; Sarcoma, Soft Tissue; Sarcoma, Uterine; Sezary Syndrome; Skin Cancer (Nonmelanoma); Skin Cancer (Melanoma); Skin Carcinoma, Merkel Cell; Small Cell Lung Cancer; Small Intestine Cancer; Soft Tissue Sarcoma; Squamous Cell Carcinoma, Squamous Neck Cancer with Occult Primary, Metastatic; Stomach (Gastric) Cancer; Supratentorial Primitive Neuroectodermal Tumors; T-Cell Lymphoma, Cutaneous; Testicular Cancer; Throat Cancer; Thymoma and Thymic Carcinoma; Thyroid Cancer; Transitional Cell Cancer of the Renal Pelvis and Ureter; Trophoblastic Tumor, Gestational; Urethral Cancer; Uterine Cancer, Endometrial; Uterine Sarcoma; Vaginal Cancer; Vulvar Cancer; Waldenstrom Macroglobulinemia; and Wilms Tumor.

In one embodiment, the cancer is acute myeloid leukemia (AML), chronic myeloid leukemia (CML), acute lymphoblastic leukemia (ALL), mantle cell lymphoma (MCL), or large B-cell lymphoma.

In one embodiment, the cancer is prostate cancer, a brain cancer, a neuroblastoma, a lung cancer, a breast cancer, a skin cancer, a cervical cancer, a colon cancer, a ovary cancer, or a pancreatic cancer.

The invention further provides methods of treating inflammatory diseases and disorders, including, for example, rheumatoid arthritis, osteoarthritis, allergies (such as asthma), and other inflammatory conditions, such as pain (such as migraine), swelling, fever, psoriasis, inflammatory bowel disease, gastrointestinal ulcers, cardiovascular conditions, including ischemic heart disease and atherosclerosis, partial brain damage caused by stroke, skin conditions (eczema, sunburn, acne), leukotriene-mediated inflammatory diseases of lungs, kidneys, gastrointestinal tract, skin, prostatitis and paradontosis.

The invention further provides methods of treating immune response disorders, whereby the immune response is inappropriate, excessive or lacking. Such disorders include allergic responses, transplant rejection, blood transfusion reaction, and autoimmune disorders including, but not limited to, Addison's disease, alopecia areata, antiphospholipid antibody syndrome (aPL), autoimmune hepatitis, celiac disease—sprue (gluten-sensitive enteropathy), dermatomyositis, Graves' disease, Guillain-Barre syndrome, Hashimoto's disease, hemolytic anemia, idiopathic thrombocytopenic purpura, inflammatory bowel disease (IBD), inflammatory myopathies, multiple sclerosis, myasthenia gravis, pernicious anemia, primary biliary cirrhosis, psoriasis, reactive arthritis, rheumatoid arthritis, scleroderma, Sjögren's syndrome, systemic lupus erythematosus, Type I diabetes and vitiligo.

The compounds disclosed herein are useful for treating cancer. Cancers treatable by the present therapy include the solid and hematological tumors, such as leukemia, breast cancer, lung cancer, prostate cancer, colon cancer, bladder cancer, liver cancer, skin cancer, brain cancer, pancreas cancer, kidney cancer, and bone cancer, comprising administering to a mammal afflicted with the cancer an amount of micheliolide derivative effective to inhibit the viability of cancer cells of the mammal. The micheliolide derivative may be administered as primary therapy, or as adjunct therapy, either following local intervention (surgery, radiation, local chemotherapy) or in conjunction with another chemotherapeutic agent. Hematological cancers, such as the leukemias are disclosed in the Mayo Clinic Family Health Book, D. E. Larson, ed., William Morrow, N.Y. (1990) and include CLL, ALL, CML and the like. Compounds of the present invention may be used in bone marrow transplant procedure to treat bone marrow prior to reintroduction to the patient. In addition, the compounds of the present invention may be used as chemotherapy sensitizers or radiation therapy sensitizers. Accordingly, a patient, or cells, or tissues, derived from a cancer patient, are pre-treated with the compounds prior to standard chemotherapy or radiation therapy.

Within another aspect of the present invention, methods are provided for inhibiting angiogenesis in patients with non-tumorigenic, angiogenesis-dependent diseases, comprising administering a therapeutically effective amount of a composition comprising micheliolide derivative to a patient with a non-tumorigenic angiogenesis-dependent disease, such that the formation of new blood vessels is inhibited. Within other aspects, methods are provided for inhibit reactive proliferation of endothelial cells or capillary formation in non-tumorigenic, angiogenesis-dependent diseases, such that the blood vessel is effectively occluded. Within one embodiment, the anti-angiogenic composition comprising micheliolide derivative is delivered to a blood vessel which is actively proliferating and nourishing a tumor.

In addition to tumors, numerous other non-tumorigenic angiogenesis-dependent diseases, which are characterized by the abnormal growth of blood vessels, may also be treated with the anti-angiogenic micheliolide derivative compositions, or anti-angiogenic factors of the present invention. Anti-angiogenic micheliolide derivative compositions of the present invention can block the stimulatory effects of angiogenesis promoters, reducing endothelial cell division, decreasing endothelial cell migration, and impairing the activity of the proteolytic enzymes secreted by the endothelium. Representative examples of such non-tumorigenic angiogenesis-dependent diseases include corneal neovascularization, hypertrophic scars and keloids, proliferative diabetic retinopathy, arteriovenous malformations, atherosclerotic plaques, delayed wound healing, hemophilic joints, nonunion fractures, Osler-Weber syndrome, psoriasis, pyogenic granuloma, scleroderma, trachoma, menorrhagia, retrolental fibroplasia and vascular adhesions. The pathology and treatment of these conditions is disclosed in detail in published PCT application PCT/CA94/00373 (WO 95/03036). Topical or directed local administration of the present compositions is often the preferred mode of administration of therapeutically effective amounts of parthenolide derivative, i.e., in depot or other controlled release forms.

Anti-angiogenic compositions of the present invention may also be utilized in a variety of other manners. For example, they may be incorporated into surgical sutures in order to prevent stitch granulomas, implanted in the uterus (in the same manner as an IUD) for the treatment of menorrhagia or as a form of female birth control, administered as either a peritoneal lavage fluid or for peritoneal implantation in the treatment of endometriosis, attached to a monoclonal antibody directed against activated endothelial cells as a form of systemic chemotherapy, or utilized in diagnostic imaging when attached to a radioactively labelled monoclonal antibody which recognizes active endothelial cells. The magnitude of a prophylactic or therapeutic dose of micheliolide derivative, an analog thereof or a combination thereof, in the acute or chronic management of cancer, i.e., prostate or breast cancer, will vary with the stage of the cancer, such as the solid tumor to be treated, the chemotherapeutic agent(s) or other anticancer therapy used, and the route of administration. The dose, and perhaps the dose frequency, will also vary according to the age, body weight, and response of the individual patient. In general, the total daily dose range for micheliolide derivative and its analogs, for the conditions described herein, is from about 0.5 mg to about 2500 mg, in single or divided doses. Preferably, a daily dose range should be about 1 mg to about 100 mg, in single or divided doses, most preferably about 5-50 mg per day. In managing the patient, the therapy should be initiated at a lower dose and increased depending on the patient's global response. It is further recommended that infants, children, patients over 65 years, and those with impaired renal or hepatic function initially receive lower doses, and that they be titrated based on global response and blood level. It may be necessary to use dosages outside these ranges in some cases. Further, it is noted that the clinician or treating physician will know how and when to interrupt, adjust or terminate therapy in conjunction with individual patient response. The terms “an effective amount” or “an effective sensitizing amount” are encompassed by the above-described dosage amounts and dose frequency schedule.

Any suitable route of administration may be employed for providing the patient with an effective dosage of micheliolide derivative (e.g., oral, sublingual, rectal, intravenous, epidural, intrathecal, subcutaneous, transcutaneous, intramuscular, intraperitoneal, intracutaneous, inhalation, transdermal, nasal spray, nasal gel or drop, and the like). While it is possible that, for use in therapy, micheliolide derivative or its analogs may be administered as the pure chemicals, as by inhalation of a fine powder via an insufflator, it is preferable to present the active ingredient as a pharmaceutical formulation. The invention thus further provides a pharmaceutical formulation comprising micheliolide derivative or an analog thereof, together with one or more pharmaceutically acceptable carriers therefor and, optionally, other therapeutic and/or prophylactic ingredients. The carrier(s) must be ‘acceptable’ in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof, such as a human patient or domestic animal.

Pharmaceutical formulations include those suitable for oral or parenteral (including intramuscular, subcutaneous and intravenous) administration. Forms suitable for parenteral administration also include forms suitable for administration by inhalation or insufflation or for nasal, or topical (including buccal, rectal, vaginal and sublingual) administration. The formulations may, where appropriate, be conveniently presented in discrete unit dosage forms and may be prepared by any of the methods well known in the art of pharmacy. Such methods include the step of bringing into association the active compound with liquid carriers, solid matrices, semi-solid carriers, finely divided solid carriers or combinations thereof, and then, if necessary, shaping the product into the desired delivery system.

Pharmaceutical formulations suitable for oral administration may be presented as discrete unit dosage forms such as hard or soft gelatin capsules, cachets or tablets each containing a predetermined amount of the active ingredient; as a powder or as granules; as a solution, a suspension or as an emulsion; or in a chewable base such as a synthetic resin or chicle for ingestion of the agent from a chewing gum. The active ingredient may also be presented as a bolus, electuary or paste. Tablets and capsules for oral administration may contain conventional excipients such as binding agents, fillers, lubricants, disintegrants, or wetting agents. The tablets may be coated according to methods well known in the art, i.e., with enteric coatings.

Oral liquid preparations may be in the form of, for example, aqueous or oily suspensions, solutions, emulsions, syrups or elixirs, or may be presented as a dry product for constitution with water or other suitable vehicle before use. Such liquid preparations may contain conventional additives such as suspending agents, emulsifying agents, non-aqueous vehicles (which may include edible oils), or preservatives.

The compounds according to the invention may also be formulated for parenteral administration (e.g., by injection, for example, bolus injection or continuous infusion) and may be presented in unit dose form in ampules, pre-filled syringes, small volume infusion containers or in multi-dose containers with an added preservative. The compositions may take such forms as suspensions, solutions, or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and/or dispersing agents. Alternatively, the active ingredient may be in powder form, obtained by aseptic isolation of sterile solid or by lyophilization from solution, for constitution with a suitable vehicle, e.g., sterile, pyrogen-free water, before use.

For topical administration to the epidermis, the compounds may be formulated as ointments, creams or lotions, or as the active ingredient of a transdermal patch. Suitable transdermal delivery systems are disclosed, for example, in Fisher et al. U.S. Pat. No. 4,788,603, or Bawa et al. U.S. Pat. Nos. 4,931,279; 4,668,506 and 4,713,224. Ointments and creams may, for example, be formulated with an aqueous or oily base with the addition of suitable thickening and/or gelling agents. Lotions may be formulated with an aqueous or oily base and will in general also contain one or more emulsifying agents, stabilizing agents, dispersing agents, suspending agents, thickening agents, or coloring agents.

Formulations suitable for topical administration in the mouth include unit dosage forms such as lozenges comprising active ingredient in a flavored base, usually sucrose and acacia or tragacanth; pastilles comprising the active ingredient in an inert base such as gelatin and glycerin or sucrose and acacia; mucoadherent gels, and mouthwashes comprising the active ingredient in a suitable liquid carrier.

When desired, the above-described formulations can be adapted to give sustained release of the active ingredient employed, e.g., by combination with certain hydrophilic polymer matrices, e.g., comprising natural gels, synthetic polymer gels or mixtures thereof. The polymer matrix can be coated onto, or used to form, a medical prosthesis, such as a stent, valve, shunt, graft, or the like.

Pharmaceutical formulations suitable for rectal administration wherein the carrier is a solid are most preferably presented as unit dose suppositories. Suitable carriers include cocoa butter and other materials commonly used in the art, and the suppositories may be conveniently formed by admixture of the active compound with the softened or melted carrier(s) followed by chilling and shaping in molds.

Formulations suitable for vaginal administration may be presented as pessaries, tampons, creams, gels, pastes, foams or sprays containing, in addition to the active ingredient, such carriers as are known in the art to be appropriate.

For administration by inhalation, the compounds according to the invention are conveniently delivered from an insufflator, nebulizer or a pressurized pack or other convenient means of delivering an aerosol spray. Pressurized packs may comprise a suitable propellant such as dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas. In the case of a pressurized aerosol, the dosage unit may be determined by providing a valve to deliver a metered amount.

Alternatively, for administration by inhalation or insufflation, the compounds according to the invention may take the form of a dry powder composition, for example, a powder mix of the compound and a suitable powder base such as lactose or starch. The powder composition may be presented in unit dosage form in, for example, capsules or cartridges or, e.g., gelatin or blister packs from which the powder may be administered with the aid of an inhalator or insufflator.

For intra-nasal administration, the compounds provided herein may be administered via a liquid spray, such as via a plastic bottle atomizer. Typical of these are the Mistometer® (Wintrop) and the Medihaler® (Riker).

For topical administration to the eye, the compounds can be administered as drops, gels (U.S. Pat. No. 4,255,415), gums (see U.S. Pat. No. 4,136,177) or via a prolonged-release ocular insert.

The term “treatment” refers to any treatment of a pathologic condition in a mammal, particularly a human, and includes: (i) preventing the pathologic condition from occurring in a subject which may be predisposed to the condition but has not yet been diagnosed with the condition and, accordingly, the treatment constitutes prophylactic treatment for the disease condition; (ii) inhibiting the pathologic condition, i.e., arresting its development; (iii) relieving the pathologic condition, i.e., causing regression of the pathologic condition; or (iv) relieving the conditions mediated by the pathologic condition.

The term “therapeutically effective amount” refers to that amount of a compound of the invention that is sufficient to effect treatment, as defined above, when administered to a mammal in need of such treatment. The therapeutically effective amount will vary depending upon the subject and disease condition being treated, the weight and age of the subject, the severity of the disease condition, the manner of administration and the like, which can readily be determined by one of ordinary skill in the art.

The term “pharmaceutically acceptable salts” includes, but is not limited to, salts well known to those skilled in the art, for example, mono-salts (e.g., alkali metal and ammonium salts) and poly salts (e.g., di- or tri-salts,) of the compounds of the invention. Pharmaceutically acceptable salts of compounds of formulas I, II, III, IV, V or VI are where, for example, an exchangeable group, such as hydrogen in —OH, —NH—, or —P(═O)(OH)—, is replaced with a pharmaceutically acceptable cation (e.g., a sodium, potassium, or ammonium ion) and can be conveniently be prepared from a corresponding compound of formula I, II, III, IV, V or VI by, for example, reaction with a suitable base. Pharmaceutically acceptable salts may be obtained using standard procedures well known in the art, for example, by reacting a sufficiently basic compound such as an amine with a suitable acid affording a physiologically acceptable anion. Alkali metal (for example, sodium, potassium or lithium) or alkaline earth metal (for example, calcium) salts of carboxylic acids can also be made.

The compounds provided herein may contain one or more chiral centers.

Accordingly, the compounds are intended to include racemic mixtures, diastereomers, enantiomers, and mixture enriched in one or more stereoisomer. When a group of substituents is disclosed herein, all the individual members of that group and all subgroups, including any isomers, enantiomers, and diastereomers are intended to be included in this disclosure. Additionally, all isotopic forms of the compounds disclosed herein are intended to be included in this disclosure. For example, it is understood that any one or more hydrogens in a molecule disclosed herein can be replaced with deuterium or tritium.

A person skilled in the art will also appreciate that starting materials, biological materials, reagents, synthetic methods, purification methods, analytical methods, assay methods, and biological methods other than those specifically exemplified can be employed in the practice of the invention. All art-known functional equivalents of any such materials and methods are intended to be included in the invention.

Unless defined otherwise herein, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure pertains.

The following examples are offered by way of illustration and not by way of limitation.

5. EXAMPLES 5.1 Example 1: Isolation of Engineered P450 Polypeptides for Micheliolide Hydroxylation

Initial studies, demonstrate that CYP102A1 variant FL #62 (SEQ ID NO: 2) is capable of efficiently oxidizing MCL, supporting about 280 total turnovers (TTN) and producing a mixture of 2(R)-hydroxy-MCL (compound 2), 14-hydroxy-MCL (compound 3), 14-CHO-MCL (compound 4) in 82:5:2 ratio (FIG. 1 and Table 1). These oxyfunctionalized derivatives of MCL provide valuable intermediates, not accessible via currently available synthetic methods, for re-elaboration of MCL scaffold by chemoenzymatic means.

A collection of FL #62-derived P450 variants prepared by active site mutagenesis (Zhang, El Damaty et al. 2011; Zhang, Shafer et al. 2012) was screened for activity on methoxy-functionalized probes derived from 2 and 3. Based on their relative activity on these MCL-based probes, selected P450 variants were tested for improved activity and selectivity toward micheliolide hydroxylation at position C2 and/or C14. Typically, micheliolide hydroxylation activity was determined by reactions with the P450 variant (1 μM in purified form or in cell lysate) in buffered solution (50 mM potassium phosphate, pH 8.0) in the presence of 1 mM parthenolide and a NADPH cofactor regeneration system (2 μM phosphite dehydrogenase, 150 μM NADP⁺, 50 mM sodium phosphite). The enzymatic reactions were extracted with dichloromethane and analyzed by gas chromatography. As described in Table 1, several P450 variants derived from CYP102A1 (SEQ ID NO: 1) or FL #62 (SEQ ID NO: 2) were found to exhibit improved activity and/or selectivity in the hydroxylation of micheliolide.

TABLE 1 % conversion Total products 2(R)—OH-MCL 14-CHO-MCL 14-OH-MCL CYP102A1 21 10 1 4 (SEQ ID NO. 1) #62 95 82 2 5 (SEQ ID NO. 2) #46 100 22 31 43 (SEQ ID NO. 3) #47 100 69 13 6 (SEQ ID NO. 4) IA1 60 43 4 7 IB1 29 22 0 6 IB3 49 44 0 4 IC3 9 6 1 1 ID1 85 76 2 6 ID3 2 1 0 0 ID5 34 26 2 5 IE3 15 11 1 3 IE8 37 24 0 12 IF5 69 61 1 5 IG1 42 26 11 4 IIA4 30 22 2 6 IIA12 10 5 4 0 IIB4 9 3 1 3 IIC1 26 22 2 2 IIE2 21 6 9 5 IIE12 21 11 9 1 IIF8 77 60 4 10 IIH8 100 64 13 22 IIIA1 11 7 1 3 IIIB5 39 23 7 7 IIIC1 29 17 2 9 IIID4 100 88 5 5 IIIG5 5 2 1 1 IVA9 55 45 3 4 IVB9 10 5 2 2 IVD3 16 13 1 1 IVF8 10 3 1 4 IVH10 52 46 1 3 VA2 34 29 1 2 VB2 27 15 2 8 VC3 4 2 1 1 VD7 47 43 1 2 VD12 5 3 0 2 VE10 33 30 1 1 VH2 100 84 9 5 VIA1 71 66 2 3 VIC9 35 21 1 12 VIE5 33 23 0 9

In addition, the following FL #62-derived variants were identified as promising catalyst for C2- or C14-hydroxylation in MCL:

Active-site mutations P450 (vs FL#62) 2-OH-MCL 14-OH-MCL V-F10 F78, A81, A82 95%  5% (SEQ ID NO. 5) V-H10 N78, F81, A82 35% 65% (SEQ ID NO. 6) VIII-B1 T74, N78, F81, F87, A180 17% 83% (SEQ ID NO. 7)

Experimental Details.

The P450 enzymes were expressed from pCWori-based vectors and purified by ion-exchange chromatography according to established procedures (Zhang, El Damaty et al. 2011; Zhang, Shafer et al. 2012). P450 concentration was determined from CO binding difference spectra (8450−500=91,000 M⁻¹ cm⁻¹). Site-saturation libraries were prepared using mutagenizing primers (NNK codon at target position) according to standard cloning procedures as described for example in (Zhang, El Damaty et al. 2011; Zhang, Shafer et al. 2012). To determine total turnover numbers and regioselectivity of the P450 variants, analytical-scale reactions (1 mL) were carried out using 0.2-1 μM P450, 1.5 mM micheliolide, 2 μM PTDH, 100 NM NADP⁺, and 50 mM sodium phosphite in potassium phosphate buffer (50 mM, pH 8.0). The P450 variants were characterized either in purified form or directly from cell lysates. After 12 hours at 4° C., the reaction mixtures were added with 500 μM guaiacol (as internal standard), extracted with dichloromethane and analyzed by gas chromatography (GC). GC analyses were carried out on a Shimadzu GC2010, an FID detector, a Restek RTX-5 column (15 m×0.25 mm×0.25μπι film), and the following separation program: 200° C. inlet, 300° C. detector, 130° C. oven, 12° C./min ramp to 290° C., and 290° C. for 2 min. TTN values were calculated based on the total amount of oxidation products as quantified based on the calibration curves generated using purified 2-4. Initial product formation rates were measured from 1 mL scale reactions containing 1 mM micheliolide, 0.1-1.0 μM purified P450, and 1 mM NADPH in potassium phosphate buffer (50 mM, pH 8.0) at room temperature. After 60 seconds, the samples were added with 500 μM Guaiacol and extracted with dichloromethane. Cofactor oxidation rate in the presence of parthenolide was measured by monitoring NADPH depletion at 340 nm (c=6.22 mM⁻¹ cm⁻¹) using 0.1-0.5 μM purified P450, 1.0 mM micheliolide, and 200 μM NADPH. Coupling efficiency was calculated from the ratio between the initial product formation rate and the initial NADPH oxidation rate.

5.2 Example 2: Synthesis of 2-Hydroxy-Micheliolide and 14-Hydroxy-Micheliolide Using Purified Enzyme

This example demonstrates how engineered P450 polypeptides provided herein are useful for enabling the synthesis of the derivative 2-hydroxy-micheliolide and 14-hydroxy-micheliolide at preparative scales (FIG. 1 ).

General Conditions for Enzymatic Reactions:

To phosphate buffer (50 mM, pH 8.0) was added P450 (2 μM), micheliolide (1 mM), NADP⁺ (150 μM), PTDH (2 μM), and sodium phosphite (50 mM, pH 8.0). After stirring for 12 hours at room temperature, the reactions were extracted with dichloromethane (3×30 mL) and separated via centrifugation. The combined organic layers were dried over sodium sulfate, concentrated under reduced pressure, and purified by silica gel flash chromatography (10 to 60% ethyl acetate in hexanes).

To prepare 2(R)-hydroxy-micheliolide (2), 14-hydroxy-micheliolide (3) and 14-CHO-micheliolide (4), purified P450 variant II-H8 (final conc: 2.5 μM; 0.26 mol %) was dissolved in 400 mL 50 mM phosphate buffer (pH 8.0) in the presence of micheliolide (100 mg, final cone: 0.95 mM), PTDH (2 μM), NADP⁺ (150 μM), and sodium phosphite (50 mM). The reaction mixture was stirred for 12 hours at 4° C. The crude product was extracted with dichloromethane (3×80 mL). The collected organic layers were dried with sodium sulfate, concentrated under vacuum, and purified by flash chromatography (hexanes/ethyl acetate: 1/2) to afford 2 (64 mg, 62%), 3 (22 mg, 21%) and 4 (13 mg, 11%). 2(R)-hydroxy-micheliolide (2): ¹H NMR (500 MHz, CDCl₃) δ=1.32 (s, 3H), 1.34-1.43 (m, 1H), 1.91-1.95 (m, 4H), 2.13 (d, 1H, J=13.8 Hz), 2.21-2.30 (m, 2H), 2.34 (dd, 2H, J=14.5, 27.1 Hz), 2.72 (t, 1H, J=9.7 Hz), 3.02 (d, 1H, J=10.3 Hz), 3.73 (t, 1H, J=10.1 Hz), 4.64 (t, 1H, J=5.8 Hz), 5.30 (s, 1H), 5.50 (d, 1H, J=1.9 Hz), 6.22 (d, 1H, J=2.7 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=24.07, 24.61, 25.86, 35.59, 48.59, 49.88, 58.52, 71.91, 77.93, 83.65, 119.60, 136.25, 138.22, 138.76, 169.45; MS (ESI) calcd for C₁₅H₂₀O₄ m/z: 264.32; found: 287.2 [M+Na]⁺, 551.2 [2M+Na]⁺, 567.2 [2M+K]⁺. The 2(R) configuration was assigned based on the observed strong NOE signal (2.6%) between the 5(H) proton and 2P(H) proton and the total absence of NOE signal between 6(H) proton and 2a(H) proton; these values were compared with the ones in MCL, where the NOE signal between the 5(H) proton and 2P(H) proton was around 3.2% and the NOE signal between 6(H) proton and 2a(H) proton was around 2.9%, therefore indicating the presence of the hydroxyl group in position 2(R). 14-hydroxy-micheliolide (3): ¹H NMR (500 MHz, CDCl₃) δ 1.27-1.36 (m, 4H), 1.74-1.80 (m, 1H), 1.84 (dd, 1H, J=7.8, 16.5 Hz), 2.13-2.21 (m, 3H), 2.26-2.36 (m, 2H), 2.52 (d, 1H, J=8.4 Hz), 2.56 (d, 1H, J=8.2 Hz), 2.61-2.73 (m, 2H), 2.80 (d, 1H, J=10.5 Hz), 3.81 (t, 1H, J=10.3 Hz), 4.08 (s, 1H), 5.51 (d, 1H, J=2.9 Hz), 6.21 (d, 1H, J=3.2 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=22.80, 25.85, 28.97, 30.35, 38.30, 50.08, 58.80, 65.53, 80.04, 84.06, 119.67, 134.32, 136.75, 138.71, 169.55; MS (ESI) calcd for C₁₅H₂₀O₄ m/z: 264.32; found: 287.2 [M+Na]⁺, 551.2 [2M+Na]⁺. 14-CHO-micheliolide (4): ¹H NMR (500 MHz, CDCl₃): δ=1.31-1.40 (m, 4H), 1.81 (t, 1H, J=15.5 Hz), 1.96-1.99 (m, 2H), 2.24 (d, 1H, J=13.5 Hz), 2.76-2.80 (m, 3H), 3.07 (d, 1H, J=10.5 Hz), 3.17 (d, 1H, J=7.0 Hz), 3.35 (d, 1H, J=3.5 Hz), 3.85 (t, 1H, J=10.5 Hz), 5.56 (s, 1H), 6.26 (s, 1H), 10.0 (s, 1H); ¹³C NMR (126 MHz, CDCl₃) δ=26.1, 26.8, 28.0, 32.3, 40.1, 48.6, 58.4, 78.9, 80.3, 122.4, 138.9, 141.2, 170.0, 173.2, 188.9; MS (ESI) calcd for C₁₅H₁₈O₄ m/z: 262.31; found: 263.4 [M+H]⁺, 285.3 [M+Na]⁺, 301.3 [M+K]⁺, 547.2 [2M+Na]⁺.

5.3 Example 3: Synthesis of 2-Hydroxy-Micheliolide and 14-Hydroxy-Micheliolide Using Whole-Cell Systems

This example demonstrates how whole-cell systems containing engineered P450 polypeptides provided herein, are useful for enabling the synthesis of the derivative 2-hydroxy-micheliolide and 14-hydroxy-micheliolide at preparative scales.

General Conditions for Whole-Cell Reactions:

E. coli cells (DH5α) were transformed with a pCWori-based plasmid encoding for the desired P450 under IPTG inducible promoter and a second, pAcyc-based plasmid encoding for the phosphite dehydrogenase (PTDH) enzyme under an arabinose-inducible promoter. Cells were grown in TB medium containing ampicillin (50 mg/L) and chloramphenicol (34 mg/L) until OD₆₀₀ reached 1.0. The cells were then induced with IPTG (0.2 mM) and arabinose (0.1%) and harvested after 24 hours. Cells were then resuspended in phosphate buffer and permeabilized via two cycles of freezing/thawing. Micheliolide (100 mg) and phosphite (50 mM) were added to the cell suspension, which was stirred for 12 hours. The micheliolide hydroxylation products were extracted using dichloromethane and purified via flash chromatography as described above.

E. coli cells expressing P450 variant II-H8 were utilized for the synthesis of 2(R)-hydroxy-micheliolide (2), 14-hydroxy-micheliolide and 14-Cho-micheliolide by incubating a suspension of these cells (from 0.5 L culture) with micheliolide (100 mg). Under unoptimized conditions, 2(R)-hydroxy-micheliolide (2) was isolated from these reactions in 58% yield, 14-hydroxy-micheliolide (3) was isolated from these reactions in 18% yield and 14-CHO-micheliolide (4) was isolated from these reactions in 6% yield.

5.4 Example 4: Synthesis of C2-Substituted Micheliolide Derivatives

This example describes and demonstrates the preparation of compounds of general formula I according to the methods provided herein. In particular, this example illustrates how C2-substituted micheliolide analogs could be prepared by coupling selective P450-catalyzed hydroxylation of the C2 site in micheliolide followed by chemical acylation (FIG. 2 ).

General Conditions for Acylation of 2(R)-Hydroxy-Micheliolide:

To a solution of compound 2 in 3 mL of anhydrous dichloromethane under argon atmosphere was added 4-dimethylaminopyridine (1 equiv.), triethylamine (5 equiv.), and the corresponding acid chloride (5 equiv.). Reaction was stirred at room temperature until complete disappearance of the starting material (ca. 2 hours). At this point, the reaction mixture was added with saturated sodium bicarbonate solution (5 mL) and extracted with dichloromethane (3×5 mL). The combined organic layers were dried over sodium sulfate, concentrated under reduced pressure, and the ester product was isolated by silica gel flash chromatography (5 to 40% ethyl acetate in hexanes). Chemical structures of representative C2-substituted derivatives prepared according to the aforementioned procedure are provided in FIG. 2 . Reagent concentration and characterization data for the 2-substituted micheliolide derivatives are provided below.

SG-05: Standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 4-(trifluoromethyl)benzoyl chloride (17 μL, 0.11 mmol). Isolated SG-05: 24 mg, 49% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.34 (s, 3H), 1.39-1.48 (m, 1H), 1.70 (s, 3H), 2.01 (dd, 1H, J=8.6, 12.5 Hz), 2.18 (d, 1H, J=11.8 Hz), 2.34-2.45 (m, 3H), 2.59 (dd, 1H, J=7.8, 12.7 Hz), 2.79 (t, 1H, J=9.3 Hz), 3.11 (d, 1H, J=8.2 Hz), 3.87 (t, 1H, J=10.1 Hz), 5.57 (d, 1H, J=2.7 Hz), 5.84 (t, 1H, J=7.5 Hz), 6.28 (d, 1H, J=3.1 Hz), 7.71 (d, 2H, J=8.1 Hz), 8.14 (d, 2H, J=8.0 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=24.15, 24.28, 25.79, 35.80, 45.52, 48.51, 58.27, 74.58, 83.95, 120.35, 125.46, 130.00 (4C), 130.86, 133.19, 134.47, 134.73, 138.26, 139.18, 164.89, 169.31; ¹⁹F NMR (376 MHz, CDCl₃): δ=−0.72; MS (ESI) calcd for C₂₃H₂₃F₃O₅ m/z: 436.43; found: 459.2 [M+Na]⁺, 895.3 [2M+Na]⁺.

SG-07: Standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 2,4-bis(trifluoromethyl)benzoyl chloride (21 μL, 0.11 mmol). Isolated SG-07: 22 mg, 39% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.33 (s, 3H), 1.39-1.47 (m, 1H), 1.74 (s, 3H), 2.06 (dd, 1H, J=8.5, 13.2 Hz), 2.16 (d, 1H, J=13.7 Hz), 2.34-2.35 (m, 2H), 2.63 (dd, 1H, J=7.8, 12.9 Hz), 2.69 (br s, 1H), 2.75 (t, 1H, J=9.6 Hz), 3.07 (d, 1H, J=9.6 Hz), 3.86 (t, 1H, J=10.1 Hz), 5.55 (d, 1H, J=1.6 Hz), 5.89 (t, 1H, J=7.4 Hz), 6.27 (d, 1H, J=2.1 Hz), 7.83 (d, 1H, J=8.0 Hz), 7.88 (d, 1H, J=8.0 Hz), 8.00 (s, 1H); ¹³C NMR (126 MHz, CDCl₃) δ=24.11, 24.26, 25.81, 35.62, 45.10, 48.26, 58.17, 75.75, 83.83, 115.01, 120.41, 124.04, 124.07, 128.75, 129.45, 129.72, 130.22, 130.45, 133.17, 133.44, 134.62, 138.19, 139.67, 165.06, 169.25, 182.96; ¹⁹F NMR (376 MHz, CDCl₃): δ=−0.86, 2.90; MS (ESI) calcd for C₂₄H₂₂F₆O₅ m/z: 504.43; found: 527.1 [M+Na]+, 543.1 [M+K]+, 1031.3 [2M+Na]+.

SG-17: Standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 3,5-bis(trifluoromethyl)benzoyl chloride (20 μL, 0.11 mmol). Isolated SG-17: 33 mg, 58% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.35 (s, 3H), 1.45 (dd, 1H, J=14.0, 26.6 Hz), 1.70 (s, 3H), 2.02 (dd, 1H, J=8.6, 12.5 Hz), 2.20 (dd, 1H, J=2.3, 13.8 Hz), 2.33-2.41 (m, 1H), 2.47 (t, 1H, J=15.2 Hz), 2.60 (dd, 1H, J=7.8, 12.8 Hz), 2.69 (s, 1H), 2.82 (t, 1H, J=10.4 Hz), 3.14 (d, 1H, J=10.3 Hz), 3.88 (t, 1H, J=10.1 Hz), 5.58 (d, 1H, J=2.9 Hz), 5.88 (t, 1H, J=7.7 Hz), 6.29 (d, 1H, J=3.3 Hz), 8.08 (s, 1H), 8.46 (s, 2H); ¹³C NMR (126 MHz, CDCl₃) δ=24.03, 24.39, 25.80, 35.71, 45.40, 48.22, 58.49, 75.46, 83.75, 120.46, 124.03, 126.84, 129.71, 130.52, 131.45, 131.95, 132.17, 132.51, 132.86, 134.30, 138.32, 139.57, 163.43, 169.23; ¹⁹F NMR (376 MHz, CDCl₃): δ=−0.51; MS (ESI) calcd for C₂₄H₂₂F₆O₅ m/z: 504.43; found: 527.2 [M+Na]⁺, 543.2 [M+K]⁺, 1031.4 [2M+Na]⁺.

SG-19: Standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and benzoyl chloride (13 μL, 0.11 mmol). Isolated SG-19: 15 mg, 36% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.25 (s, 3H), 1.34 (dd, 1H, J=9.3, 15.8 Hz), 1.70 (s, 3H), 2.01 (dd, 1H, J=8.7, 13.4 Hz), 2.18 (d, 1H, J=11.4 Hz), 2.34-2.42 (m, 2H), 2.60 (dd, 1H, J=9.1, 16.3 Hz), 2.67 (bs s, 1H), 2.78 (t, 1H, J=10.7), 3.11 (d, 1H, J=8.9 Hz), 3.85 (t, 1H, J=10.1 Hz), 5.52 (d, 1H, J=7.2 Hz), 5.84 (t, 1H, J=9.4 Hz), 6.23 (d, 1H, J=4.9 Hz), 7.45 (t, 2H, J=11.4 Hz), 7.57 (t, 1H, J=10.8 Hz), 8.03 (d, 2H, J=9.8 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=22.8, 25.7, 38.2, 45.5, 50.0, 58.9, 74.5, 83.6, 119.7, 128.4 (2C), 128.7, 129.5 (2C), 130.0, 133.1, 138.5, 138.9, 139.2, 140.0, 166.5, 169.4; MS (ESI) calcd for C₂₂H₂₄O₅ m/z: 368.43; found: 391.3 [M+Na]⁺, 759.3 [M+Na]⁺.

SG-20: Standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 4-fluorobenzoyl chloride (13 μL, 0.11 mmol). Isolated SG-20: 17 mg, 38% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.34 (s, 3H), 1.44 (dd, 1H, J=11.1, 22.5 Hz), 1.70 (s, 3H), 1.99 (dd, 1H, J=8.6, 12.6 Hz), 2.17 (dd, 1H, J=2.3, 13.8 Hz), 2.30-2.47 (m, 3H), 2.57 (dd, 1H, J=7.8, 12.7 Hz), 2.77 (t, 1H, J=10.5 Hz), 3.09 (dd, 1H, J=2.2, 10.2 Hz), 3.86 (t, 1H, J=10.2 Hz), 5.55 (t, 1H, J=7.1 Hz), 5.80 (t, 1H, J=7.7 Hz), 6.27 (d, 1H, J=3.3 Hz), 7.05-7.16 (m, 2H), 8.04 (dd, 2H, J=5.5, 8.7 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=24.07, 24.27, 25.80, 35.79, 45.80, 48.55, 58.35, 74.27, 84.00, 115.75 (2C), 120.51, 126.21, 131.18, 132.27 (2C), 138.39, 139.02, 164.84, 165.35, 167.04, 169.45; ¹⁹F NMR (376 MHz, CDCl₃): δ −43.0; MS (ESI) calcd for C₂₂H₂₃FO₅ m/z: 386.42; found: 409.3 [M+Na]⁺, 425.2 [M+K]⁺, 795.4 [2M+Na]⁺, 811.4 [2M+K]⁺.

SG-21: Standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 4-(dimethylamino)benzoyl chloride (21 mg, 0.11 mmol). Isolated SG-21: 9 mg, 18% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.31-1.39 (m, 4H), 1.69 (s, 3H), 1.88 (dd, 1H, J=8.4, 15.3 Hz), 1.91 (dd, 1H, J=9.3, 11.2 Hz), 2.12-2.25 (m, 1H), 2.42 (t, 1H, J=10.8 Hz), 2.58-2.62 (m, 1H), 2.65-2.73 (m, 2H), 2.85 (d, 1H, J=8.8 Hz), 3.04 (s, 6H), 3.85 (t, 1H, J=7.6 Hz), 5.50 (s, 1H), 5.80 (t, 1H, J=11.6 Hz), 6.22 (d, 1H, J=5.7 Hz), 6.66 (d, 2H, J=12.4 Hz), 7.89 (d, 2H, J=11.9 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=22.8, 25.7, 293, 30.7, 38.2, 40.1 (2C), 45.1, 50.1, 58.9, 72.8, 83.8, 110.8, 114.2, 119.6, 122.4, 130.6, 131.3 (2C), 138.6, 139.1, 153.3, 166.8, 169.5; MS (ESI) calcd for C₂₄H₂₉NO₅ m/z: 411.50; found: 434.3 [M+Na]⁺, 450.2 [M+K]⁺, 845.4 [2M+Na]⁺, 861.2 [2M+K]⁺.

SG-23: Standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 1-methylindole-3-carbonyl chloride (21 mg, 0.11 mmol), previously synthesized as described. Isolated SG-23: 18 mg, 37% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.53 (s, 3H), 1.59-1.63 (m, 1H), 1.84 (s, 3H), 2.15 (dd, 1H, J=6.4, 15.2 Hz), 2.28 (d, 1H, J=11.4 Hz), 2.42-2.54 (m, 2H), 2.68 (dd, 1H, J=9.7, 18.4 Hz), 2.84 (t, 1H, J=7.6 Hz), 3.15 (d, 1H, J=6.7 Hz), 3.82-3.94 (m, 5H), 5.51 (d, 1H, J=4.2 Hz), 5.88 (t, 1H, J=11.5 Hz), 6.22 (d, 1H, J=3.7 Hz), 7.28-7.37 (m, 3H), 7.79 (s, 1H), 8.10 (d, 1H, J=12.4 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=22.8, 25.7, 29.3, 30.9, 33.5, 38.3, 45.1, 50.1, 58.9, 60.4, 72.3, 83.8, 109.9, 119.6, 121.5, 122.0, 122.9, 126.5, 130.6, 135.3, 137.2, 138.6, 139.2, 164.9, 169.5; MS (ESI) calcd for C₂₅H₂₇NO₅ m/z: 421.49; found: 444.3 [M+Na]⁺, 865.5 [2M+Na]⁺.

SG-27: Standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 2-naphthylcarbonyl chloride (21 mg, 0.11 mmol), previously synthesized as described. Isolated SG-27: 20 mg, 41% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.37 (s, 3H), 1.41 (q, 1H, J=9.5 Hz), 1.74 (s, 3H), 2.08 (dd, 1H, J=6.4, 18.5 Hz), 2.18 (d, 1H, J=12.4 Hz), 2.37 (d, 1H, J=13.3 Hz), 2.47 (t, 1H, J=11.0 Hz), 2.61 (dd, 1H, J=6.7, 15.8 Hz), 2.82 (t, 1H, J=9.7 Hz), 3.14 (d, 1H, J=11.8 Hz), 3.89 (t, 1H, J=10.5 Hz), 5.57 (d, 1H, J=3.4 Hz), 5.89 (t, 1H, J=8.8 Hz), 6.28 (d, 1H, J=4.1 Hz), 7.53-7.61 (m, 2H), 7.88 (d, 2H, J=8.5 Hz), 7.96 (d, 1H, J=8.6 Hz), 8.04 (d, 1H, J=9.1 Hz), 8.58 (s, 1H); ¹³C NMR (126 MHz, CDCl₃) δ=24.2, 24.3, 25.8, 35.8, 45.6, 48.6, 58.3, 74.0, 84.0, 120.2, 125.2, 126.7, 127.2, 127.7, 128.2, 128.3, 129.3, 129.5, 131.0, 131.1, 132.5, 135.5, 138.3, 138.9, 166.2, 169.4; MS (ESI) calcd for C₂₆H₂₆O₅ m/z: 418.49; found: 441.4 [M+Na]⁺, 457.3 [M+K]⁺, 859.6 [2M+Na]⁺, 875.4 [2M+K]⁺.

SG-31: Standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 5-phenylpyrazole-4-carbonyl chloride (23 mg, 0.11 mmol), previously synthesized as described. Isolated SG-31: 6 mg, 12% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.37 (s, 3H), 1.51 (dd, 2H, J=6.6, 18.9 Hz), 1.74 (s, 3H), 2.06 (dd, 1H, J=7.2, 14.9 Hz), 2.18 (d, 1H, J=10.5 hz), 2.35-2.52 (m, 3H), 2.62 (dd, 3H, J=9.4, 15.7 Hz), 2.81 (t, 1H, J=8.9 Hz), 3.19 (d, 1H, J=10.2 Hz), 3.89 (t, 1H, J=10.5 Hz), 5.49 (d, 1H, J=9.5 Hz), 6.22 (d, 1H, J=9.8 Hz), 7.38-7.49 (m, 3H), 7.61-7.68 (m, 2H), 8.06 (s, 1H); ¹³C NMR (126 MHz, CDCl₃) δ=22.2, 22.6, 25.6, 30.2, 30.8, 38.2, 50.0, 59.2, 72.8, 83.2, 111.0, 119.7, 128.1 (2C), 128.2, 129.1 (2C), 129.3, 129.6, 129.9, 132.5, 139.8, 140.4, 163.0, 169.9; MS (ESI) calcd for C₂₅H₂₆N₂O₅ m/z: 434.49; found: 457.3 [M+Na]⁺, 473.3 [M+K]⁺, 891.5 [2M+Na]⁺, 907.5 [2M+K]⁺.

SG-33: Standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 5-(2-(trifluoromethyl)phenyl)furan-2-carbonyl chloride (30 mg, 0.11 mmol), previously synthesized as described. Isolated SG-33: 22 mg, 38% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.32 (s, 3H), 1.42 (dd, 1H, J=10.5, 19.4 Hz), 1.74 (s, 3H), 2.03 (dd, 1H, J=3.5, 11.4 Hz), 2.17 (d, 1H, J=15.0 Hz), 2.33-2.41 (m, 2H), 2.57 (dd, 2H, J=5.2, 12.8 Hz), 2.77 (t, 1H, J=9.5 Hz), 3.10 (d, 1H, J=10.5 Hz), 3.85 (t, 1H, J=10.5 Hz), 5.56 (d, 1H, J=3.0 Hz), 5.80 (t, 1H, J=8.8 Hz), 6.27 (d, 1H, J=3.0 Hz), 6.75 (d, 1H, J=4.2 hz), 7.26 (d, 1H, J=3.9 Hz), 7.51 (t, 1H, J=7.5 Hz), 7.62 (t, 1H, J=7.5 Hz), 7.76-7.84 (m, 2H); ¹³C NMR (126 MHz, CDCl₃) δ=24.2, 24.3, 25.8, 29.3, 35.7, 45.4, 48.5, 58.2, 74.1, 84.0, 119.5, 120.2, 122.4, 125.8, 129.1, 130.7, 130.8, 130.9, 131.8, 132.5, 133.3, 138.3, 139.2, 143.8, 144.8, 158.2, 169.4; ¹⁹F NMR (376 MHz, CDCl₃): δ=−11.3; MS (ESI) calcd for C₂₇H₂₅F₃O₆ m/z: 502.49; found: 525.1 [M+Na]⁺, 541.1 [M+K]⁺, 1027.3 [2M+Na]⁺, 1043.2 [2M+K]⁺.

5.5 Example 5: Synthesis of C14-Substituted Micheliolide Derivatives

This example describes and demonstrates the preparation of compounds of general formula II according to the methods provided herein. In particular, this example illustrates how C14-substituted micheliolide analogs could be prepared by coupling selective P450-catalyzed hydroxylation of the C14 site in micheliolide followed by chemical acylation (FIG. 3 ).

General Conditions for Acylation of 14-Hydroxy-Micheliolide:

To a solution of compound 3 in 3 mL of anhydrous dichloromethane under argon atmosphere was added 4-dimethylaminopyridine (1 equiv.), triethylamine (5 equiv.), and the corresponding acid chloride (5 equiv.). Reaction was stirred at room temperature until complete disappearance of the starting material (ca. 2 hours). At this point, the reaction mixture was added with saturated sodium bicarbonate solution (5 mL) and extracted with dichloromethane (3×5 mL). The combined organic layers were dried over sodium sulfate, concentrated under reduced pressure, and the ester product was isolated by silica gel flash chromatography (5 to 40% ethyl acetate in hexanes). Chemical structures of representative C14-substituted derivatives prepared according to the aforementioned procedure are provided in FIG. 3 . Reagent concentration and characterization data for the 14-substituted micheliolide derivatives are provided below.

SG-04: To a solution of 14-OH-MCL (30 mg, 0.11 mmol) in 3 mL of anhydrous DCM under Ar atmosphere was added 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and benzoyl chloride (13 μL, 0.11 mmol). Reaction was stirred at r.t (or at 40° C. if needed) until disappearance of the starting material (from 2 to 72 h). At this point, the reaction mixture was added with saturated sodium bicarbonate solution (5 mL) and extracted with DCM (3×5 mL). The combined organic layers were dried over Na₂S₂O₄, concentrated under reduced pressure, and the ester product was isolated by flash chromatography on silica gel (eluting mixture from 5% EtOAc in n-Hexane to 40% EtOAc in n-Hexane) to obtain 20 mg of the desired product (48% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.32-1.40 (m, 1H), 1.35 (s, 3H), 1.81-1.86 (m, 1H), 1.87-1.92 (m, 1H), 2.18 (d, 1H, J=13.5 Hz), 2.27 (t, 1H, J=14.2 Hz), 2.40-2.48 (m, 2H), 2.61 (d, 1H, J=16.1 Hz), 2.66-2.74 (m, 2H), 2.86 (d, 1H, J=10.6 Hz), 3.86 (t, 1H, J=10.3 Hz), 4.78 (s, 2H), 5.52 (d, 1H, J=2.9 Hz), 6.23 (d, 1H, J=3.2 Hz), 7.45 (t, 2H, J=7.4 Hz), 7.57 (t, 1H, J=7.4 Hz), 8.03 (d, 2H, J=7.6 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=22.87, 25.70, 29.38, 30.86, 38.25, 50.06, 58.98, 67.65, 80.12, 83.69, 119.72, 128.46 (2C), 129.60 (2C), 130.04, 130.13, 133.10, 138.52, 140.01, 166.54, 169.46; MS (ESI) calcd for C₂₂H₂₄O₅ m/z: 368.43; found: 391.3 [M+Na]⁺, 407.2 [M+K]⁺, 759.3 [2M+Na]⁺.

SG-06: Standard procedure was applied using 14-OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 4-(trifluoromethyl)benzoyl chloride (17 μL, 0.11 mmol). Isolated SG-06: 37 mg, 74% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.32-1.38 (m, 4H), 1.81-1.93 (m, 2H), 2.19 (d, 1H, J=13.5 Hz), 2.28 (t, 1H, J=14.2 Hz), 2.40-2.48 (m, 1H), 2.58 (d, 1H, J=16.3 Hz), 2.68 (d, 1H, J=8.5 Hz) 2.70-2.74 (m, 1H), 2.87 (d, 1H, J=10.5 Hz), 3.85 (t, 1H, J=10.3 Hz), 4.82 (s, 2H), 5.52 (d, 1H, J=2.7 Hz), 6.23 (d, 1H, J=3.1 Hz), 7.71 (d, 2H, J=8.1 Hz), 8.14 (d, 2H, J=8.0 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=22.86, 25.69, 29.42, 30.89, 38.22, 50.03, 59.01, 68.22, 80.10, 83.57, 119.78, 124.67, 125.52, 129.58, 130.01 (4C), 133.33, 138.50, 140.65, 165.31, 169.38; ¹⁹F NMR (376 MHz, CDCl₃): δ=−0.73; MS (ESI) calcd for C₂₃H₂₃F₃O₅ m/z: 436.43; found: 459.2 [M+Na]⁺, 475.2 [M+K]⁺, 895.4 [2M+Na]⁺.

SG-08: Standard procedure was applied using 14-OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 2,4-bis(trifluoromethyl)benzoyl chloride (21 μL, 0.11 mmol). Isolated SG-08: 35 mg, 60% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.30-1.38 (m, 4H), 1.80-1.91 (m, 2H), 2.17 (d, 1H, J=13.1 Hz), 2.28 (t, 1H, J=14.3 Hz), 2.40-2.48 (m, 1H), 2.54 (d, 1H, J=16.1 Hz), 2.63-2.73 (m, 3H), 2.85 (d, 1H, J=10.5 Hz), 3.83 (t, 1H, J=10.3 Hz), 4.77 (d, 1H, J=11.5 Hz), 4.87 (d, 1H, J=11.5 Hz), 5.52 (d, 1H, J=1.5 Hz), 6.23 (d, 1H, J=1.9 Hz), 7.89 (s, 2H), 7.99 (s, 1H); ¹³C NMR (126 MHz, CDCl₃) δ=22.77, 25.62, 29.38, 31.36, 38.14, 49.89, 59.04, 69.62, 80.07, 83.54, 119.83, 124.01, 128.87, 128.94, 129.32, 129.53, 130.93, 133.28, 133.55, 134.60, 138.38, 141.75, 165.84, 169.38; ¹⁹F NMR (376 MHz, CDCl₃): δ=−0.86, 2.72; MS (ESI) calcd for C₂₄H₂₂F₆O₅ m/z: 504.43; found: 527.1 [M+Na]⁺, 543.1 [M+K]⁺, 1031.3 [2M+Na]⁺.

SG-09: Standard procedure was applied using 14-OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 4-(dimethylamino)benzoyl chloride (21 mg, 0.11 mmol). Isolated SG-09: 19 mg, 41% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.31-1.39 (m, 4H), 1.79-1.91 (m, 2H), 2.16 (d, 1H, J=12.1 Hz), 2.23 (t, 1H, J=14.4 Hz), 2.38-2.46 (m, 1H), 2.58-2.73 (m, 4H), 2.85 (d, 1H, J=10.5 Hz), 3.04 (s, 6H), 3.85 (t, 1H, J=10.3 Hz), 5.51 (d, 1H, J=2.6 Hz), 6.22 (d, 1H, J=3.1 Hz), 6.66 (d, 2H, J=8.5 Hz), 7.89 (d, 2H, J=8.8 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=22.89, 25.71, 29.33, 30.73, 38.39, 40.24 (2C), 50.18, 58.93, 66.82, 80.08, 83.82, 110.87, 119.62, 130.67, 131.31 (4C), 138.71, 139.05, 153.31, 166.87, 169.62; MS (ESI) calcd for C₂₄H₂₉NO₅ m/z: 411.50; found: 434.3 [M+Na]⁺, 450.2 [M+K]⁺, 845.4 [2M+Na]⁺, 861.2 [2M+K]⁺.

SG-11: Standard procedure was applied using 14-OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 4-fluorobenzoyl chloride (13 μL, 0.11 mmol). Isolated SG-11: 26 mg, 61% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.32-1.39 (m, 4H), 1.80-1.92 (m, 2H), 2.16-2.19 (m, 2H), 2.26 (t, 1H, J=20.0 Hz), 2.40-2.47 (m, 1H), 2.58 (d, 1H, J=16.0 Hz), 2.64-2.74 (m, 2H), 2.86 (d, 1H, J=10.2 Hz), 3.85 (t, 1H, J=10.3 Hz), 2.41 (s, 2H), 5.52 (d, 1H, J=2.8 Hz), 6.23 (d, 1H, J=3.1 Hz), 7.12 (t, 2H, J=8.5 Hz), 8.05 (dd, 2H, J=3.4, 10.6 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=22.87, 25.69, 29.39, 30.87, 38.23, 50.05, 58.99, 67.79, 80.11, 83.64, 115.54, 115.71, 119.75, 126.36, 129.88, 132.11, 132.18 (2C), 138.47, 140.22, 166.22 (d, J=161.6 Hz), 169.25; ¹⁹F NMR (376 MHz, CDCl₃): δ=−42.93; MS (ESI) calcd for C₂₂H₂₃FO₅ m/z: 386.42; found: 409.2 [M+Na]⁺, 425.2 [M+K]⁺, 795.3 [2M+Na]⁺.

SG-16: Standard procedure was applied using 14-OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 3,5-bis(trifluoromethyl)benzoyl chloride (20 μL, 0.11 mmol). Isolated SG-16: 42 mg, 79% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.29-1.41 (m, 4H), 1.80-1.88 (m, 1H), 1.91 (dd, 1H, J=7.9, 16.6 Hz), 2.20 (d, 1H, J=13.6 Hz), 2.29 (t, 1H, J=14.2 Hz), 2.46 (dt, 1H, J=12.6, 16.7 Hz), 2.57 (dd, 1H, J=2.5, 15.9 Hz), 2.64-2.78 (m, 3H), 2.88 (d, 1H, J=10.6 Hz), 3.86 (t, 1H, J=10.3 Hz), 4.81-4.91 (m, 2H), 5.52 (d, 1H, J=2.9 Hz), 6.23 (d, 1H, J=3.2 Hz), 8.07 (s, 1H), 8.45 (s, 2H); ¹³C NMR (126 MHz, CDCl₃) δ=22.85, 25.69, 29.56, 30.78, 38.19, 49.96, 58.97, 68.96, 80.03, 83.47, 119.99, 121.56, 123.86, 126.49, 128.94, 129.70, 131.92, 132.27, 132.43, 132.82, 138.23, 141.31, 163.79, 169.25; ¹⁹F NMR (376 MHz, CDCl₃): δ=−0.57; MS (ESI) calcd for C₂₄H₂₂F₆O₅ m/z: 504.43; found: 527.2 [M+Na]⁺, 543.2 [M+K]⁺, 1031.4 [2M+Na]⁺.

SG-22: Standard procedure was applied using 14-OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 1-methylindole-3-carbonyl chloride (21 mg, 0.11 mmol). The acid chloride was freshly synthesized as follows: to a suspension of 1-methylindole-3-carboxylic acid (100 mg, 0.57 mmol) in 5 mL of anhydrous toluene under Ar atmosphere was added thionyl chloride (62 μL, 0.86 mmol) and the reaction mixture was stirred under reflux for 12 h, then cooled at r.t. and evaporated under reduced pressure. The remaining residue was used without any further purification in the next step. Isolated SG-22: 27 mg, 56% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.37-1.42 (m, 4H), 1.59 (br s, 1H), 1.83 (dd, 1H, J=7.8, 15.4 Hz), 1.89 (dd, 1H, J=6.5, 12.8 Hz), 2.20 (d, 1H, J=11.4 Hz), 2.29 (t, 1H, J=10.6 Hz), 2.41-2.52 (m, 1H), 2.64 (s, 1H), 2.69-2.78 (m, 2H), 2.84 (d, 1H, J=9.5 Hz), 3.82-3.89 (m, 4H), 4.79 (s, 2H), 5.51 (d, 1H, J=4.8 Hz), 6.22 (d, 1H, J=5.1 Hz), 7.28-7.33 (m, 2H), 7.36 (d, 1H, J=9.4 Hz), 7.79 (s, 1H), 8.11 (d, 1H, J=9.4 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=22.8, 25.7, 29.3, 30.9, 33.5, 38.3, 50.1, 60.4, 66.3, 80.1, 83.8, 106.8, 109.9, 119.6, 121.5, 122.0, 122.9, 126.5, 130.6, 135.3, 137.2, 138.6, 139.2, 164.9, 169.5; MS (ESI) calcd for C₂₅H₂₇NO₅ m/z: 421.49; found: 444.3 [M+Na]⁺, 465.5 [2M+Na]+, 881.3 [2M+K]⁺.

SG-26: Standard procedure was applied using 14-OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 2-naphthylcarbonyl chloride (21 mg, 0.11 mmol), previously synthesized as described. Isolated SG-26: 33 mg, 69% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.34-1.42 (m, 4H), 1.89 (dd, 1H, J=6.3, 12.4 Hz), 1.92 (dd, 1H, J=9.4, 15.3 Hz), 2.20 (d, 1H, J=13.5 Hz), 2.30 (t, 1H, J=15.0 Hz), 2.46-2.48 (m, 1H), 2.65-2.67 (m, 2H), 2.70-2.75 (m, 2H), 2.88 (d, 1H, J=10.5 Hz), 3.87 (t, 1H, J=10.5 Hz), 4.85 (s, 2H), 5.52 (d, 1H, J=2.5 Hz), 6.23 (d, 1H, J=3.2 Hz), 7.55 (t, 1H, J=8.9 Hz), 7.60 (t, 1H, J=9.4 Hz), 7.89 (d, 2H, J=10.5 Hz), 7.96 (d, 1H, J=8.8 Hz), 8.04 (d, 1H, J=9.3 Hz), 8.59 (s, 1H); ¹³C NMR (126 MHz, CDCl₃) δ=22.9, 25.7, 29.4, 30.8, 38.2, 50.0, 59.0, 67.7, 80.1, 83.7, 119.7, 125.1, 126.7, 127.3, 127.8, 128.2, 128.3, 129.3, 130.0, 131.1, 132.4, 135.5, 138.5, 140.0, 166.7, 169.4; MS (ESI) calcd for C₂₆H₂₆O₅ m/z: 418.49; found: 441.4 [M+Na]⁺, 457.3 [M+K]⁺, 859.6 [2M+Na]⁺, 875.5 [2M+K]⁺.

SG-30: Standard procedure was applied using 14-OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 5-phenylpyrazole-4-carbonyl chloride (23 mg, 0.11 mmol), previously synthesized as described. Isolated SG-30: 17 mg, 34% yield. ¹H NMR (500 MHz, CDCl₃): C=1.18 (q, 1H, J=8.8 Hz), 1.32 (s, 3H), 1.72-1.88 (m, 2H), 1.96-2.14 (m, 3H), 2.35-2.42 (m, 3H), 2.54 (dd, 1H, J=5.6, 17.4 Hz), 2.68 (t, 1H, J=9.8 Hz), 2.80 (d, 1H, J=10.5 Hz), 3.77 (t, 1H, J=10.5 Hz), 4.63 (s, 2H); 5.49 (d, 1H, J=4.4 Hz), 6.22 (d, 1H, J=4.2 Hz), 7.40-7.45 (m, 3H), 7.62-7.69 (m, 2H), 8.06 (s, 1H); ¹³C NMR (126 MHz, CDCl₃) δ=22.8, 25.5, 29.2, 30.8, 38.2, 50.0, 58.8, 66.8, 80.0, 83.7, 11.0, 114.9, 119.7, 128.1 (2C), 129.2 (2C), 129.5, 129.6, 129.9, 138.5, 139.8, 140.4, 163.1, 169.6; MS (ESI) calcd for C₂₅H₂₆N₂O₅ m/z: 434.49; found: 457.3 [M+Na]⁺, 473.3 [M+K]⁺, 869.6 [2M+H]⁺, 891.5 [2M+Na]⁺, 907.5 [2M+K]⁺.

SG-32: Standard procedure was applied using 14-hydroxy-micheliolide (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 5-(2-(trifluoromethyl)phenyl)furan-2-carbonyl chloride (30 mg, 0.11 mmol), previously synthesized as described. Isolated SG-32: 35 mg, 62% yield. ¹H NMR (500 MHz, CDCl₃): C=1.35-1.39 (m, 4H), 1.80-1.89 (m, 2H), 2.16-2.35 (m, 2H), 2.39-2.51 (m, 1H), 2.62 (d, 2H, J=15.2 Hz), 2.70 (dd, 2H, J=6.8, 16.7 Hz), 2.85 (d, 1H, J=10.5 Hz), 3.85 (t, 1H, J=10.5 Hz), 4.78 (dd, 2H, J=8.8, 15.3 Hz), 5.52 (d, 1H, J=2.5 Hz), 6.23 (d, 1H, J=3.0 Hz), 6.78 (d, 1H, J=3.0 Hz), 7.26 (d, 1H, J=2.9 Hz), 7.52 (t, 1H, J=7.5 Hz), 7.62 (t, 1H, J=8.0 Hz), 7.79 (t, 2H, J=7.5 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=22.8, 25.6, 29.3, 29.7, 30.7, 38.2, 50.0, 58.9, 67.5, 80.1, 83.6, 111.8, 119.5, 119.7, 126.7, 127.4, 128.8, 129.1, 129.7, 130.6, 131.9, 138.5, 140.3, 144.4, 154.1, 158.5, 169.4; ¹⁹F NMR (376 MHz, CDCl₃): δ=−3.15; MS (ESI) calcd for C₂₇H₂₅F₃O₆ m/z: 502.49; found: 525.3 [M+Na]⁺, 541.3 [M+K]⁺, 1043.3 [2M+K]⁺.

5.6 Example 6: Synthesis of C2,C4-Di-Substituted Micheliolide Derivatives

This example describes and demonstrates the preparation of compounds of general formula III according to the methods provided herein. In particular, this example illustrates how C2,C4-disubstituted micheliolide analogs could be prepared by coupling selective P450-catalyzed hydroxylation of the C2 site in micheliolide followed by chemical acylation (FIG. 4 ).

General Conditions for Acylation of 2,4-Di-Hydroxy-Micheliolide:

To a solution of compound 2 in 3 mL of anhydrous dichloromethane under argon atmosphere was added 4-dimethylaminopyridine (1 equiv.), triethylamine (5 equiv.), and the corresponding acid chloride (5 equiv.). Reaction was stirred at room temperature until complete disappearance of the starting material (from 2 to 12 hours). At this point, the reaction mixture was added with saturated sodium bicarbonate solution (5 mL) and extracted with dichloromethane (3×5 mL). The combined organic layers were dried over sodium sulfate, concentrated under reduced pressure, and the ester product was isolated by silica gel flash chromatography (5 to 40% ethyl acetate in hexanes). Chemical structures of representative C2,C4-disubstituted derivatives prepared according to the aforementioned procedure are provided in FIG. 4 . Reagent concentration and characterization data for the 2,4-di-substituted micheliolide derivatives are provided below.

SG-12: Standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 3,5-bis(trifluoromethyl)benzoyl chloride (101 μL, 0.56 mmol). Isolated SG-12: 18 mg, 21% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.53 (dd, 1H, J=10.2, 21.5 Hz), 1.72 (s, 3H), 1.77 (s, 3H), 2.26 (d, 1H, J=13.8 Hz), 2.42-2.46 (m, 2H), 2.50-2.60 (m, 1H), 2.94 (t, 1H, J=9.0 Hz), 3.33 (dd, 1H, J=7.9, 13.7 Hz), 3.68 (d, 1H, J=8.8 Hz), 3.95 (t, 1H, J=10.0 Hz), 5.58 (d, 1H, J=2.4 Hz), 5.99 (t, 1H, J=6.6 Hz), 6.30 (d, 1H, J=2.9 Hz), 8.03 (s, 1H), 8.05 (s, 1H), 8.40 (s, 2H), 8.47 (s, 2H); ¹³C NMR (126 MHz, CDCl₃) δ=20.27, 24.21, 25.95, 35.68, 43.55, 48.64, 56.88, 75.44, 81.88, 87.16, 119.97, 121.69, 121.78, 123. 129.61, 89, 123.95, 126.28, 126.33, 126.59, 128.25, 129.73, 129.87, 131.96, 132.03, 132.17, 132.30, 132.44, 133.19, 138.49, 141.49, 163.04, 163.36, 169.29; ¹⁹F NMR (376 MHz, CDCl₃): δ=−0.57 (4F); MS (ESI) calcd for C₃₃H₂₄F₁₂O₆ m/z: 744.53; found: 767.2 [M+Na]⁺.

SG-25: Standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 1-methylindole-3-carbonyl chloride (105 mg, 0.56 mmol), previously synthesized as described. Isolated SG-25: 11 mg, 17% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.38-1.50 (m, 1H), 1.62 (s, 3H), 1.69 (s, 3H), 2.14-2.22 (m, 2H), 2.27-2.41 (m, 1H), 2.52-2.63 (m, 1H), 2.64-2.70 (m, 1H), 2.70-2.86 (m, 2H), 3.37 (d, 1H, J=12.4 Hz), 3.81 (s, 3H), 3.82 (s, 3H), 3.92 (t, 1H, J=10.2 Hz), 5.52 (d, 1H, J=4.2 Hz), 5.89 (d, 1H, J=5.4 Hz), 7.27-7.39 (m, 6H), 7.82 (s, 1H), 7.92 (s, 1H), 8.16 (d, 1H, J=12.4 Hz), 8.26 (dd, 1H, J=9.4, 17.5 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=19.0, 19.1, 25.9, 29.7, 30.0, 31.0 (2C), 33.4, 37.1, 45.6, 50.6, 57.9, 74.5, 87.7, 106.8, 107.9, 109.6, 109.9, 118.8, 121.5, 121.7, 122.0, 122.5, 122.8, 126.5, 126.8, 131.1, 135.4, 136.0, 137.2, 137.6, 139.3, 164.3, 164.9, 170.1; MS (ESI) calcd for C₃₅H₃₄N₂O₆ m/z: 578.67; found: 601.3 [M+Na]⁺, 1179.5 [2M+Na]⁺.

SG-29: Standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 2-naphthylcarbonyl chloride (105 mg, 0.56 mmol), previously synthesized as described. Isolated SG-29: 23 mg, 36% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.47 (s, 3H), 1.67 (q, 1H, J=12.5 Hz), 1.77 (s, 3H), 2.12-2.28 (m, 2H), 2.41 (t, 1H, J=11.4 Hz), 2.56-2.63 (m, 1H), 2.71 (d, 1H, J=13.2 Hz), 2.82-2.96 (m, 1H), 3.47 (d, 1H, J=14.1 Hz), 4.04 (t, 1H, J=15.5 Hz), 5.54 (d, 1H, J=3.9 Hz), 5.92 (t, 1H, J=9.8 Hz), 6.28 (d, 1H, J=3.4 Hz), 7.51-7.62 (m, 4H), 7.80-7.90 (m, 4H), 7.92-8.09 (m, 4H), 8.62 (s, 1H), 8.72 (s, 1H); ¹³C NMR (126 MHz, CDCl₃) δ=18.6, 18.7, 25.9, 30.0, 31.0, 36.7, 50.4, 57.9, 67.9, 82.2, 88.7, 119.1, 125.1, 125.3, 126.4, 126.7, 127.6, 127.8, 128.0, 128.1, 128.4, 128.7, 129.3, 129.6, 130.8, 130.9, 131.1, 131.4, 132.5, 132.6, 133.5, 135.4, 135.6, 137.8, 139.1, 166.3, 166.7; MS (ESI) calcd for C₃₇H₃₂O₆ m/z: 572.66; found: 595.2 [M+Na]⁺, 1167 [2M+Na]⁺.

5.7 Example 7: Synthesis of C4,C14-Di-Substituted Micheliolide Derivatives

This example describes and demonstrates the preparation of compounds of general formula IV according to the methods provided herein. In particular, this example illustrates how C4,C14-disubstituted micheliolide analogs could be prepared by coupling selective P450-catalyzed hydroxylation of the C14 site in micheliolide followed by chemical acylation (FIG. 4 ).

General Conditions for Acylation of 4,14-Di-Hydroxy-Micheliolide:

To a solution of compound 3 in 3 mL of anhydrous dichloromethane under argon atmosphere was added 4-dimethylaminopyridine (1 equiv.), triethylamine (5 equiv.), and the corresponding acid chloride (5 equiv.). Reaction was stirred at room temperature until complete disappearance of the starting material (from 2 to 12 hours). At this point, the reaction mixture was added with saturated sodium bicarbonate solution (5 mL) and extracted with dichloromethane (3×5 mL). The combined organic layers were dried over sodium sulfate, concentrated under reduced pressure, and the ester product was isolated by silica gel flash chromatography (5 to 40% ethyl acetate in hexanes). Chemical structures of representative C4,C14-disubstituted derivatives prepared according to the aforementioned procedure are provided in FIG. 4 . Reagent concentration and characterization data for the 4,14-di-substituted micheliolide derivatives are provided below.

SG-10: Standard procedure was applied using 14-OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 3,5-bis(trifluoromethyl)benzoyl chloride (101 μL, 0.56 mmol). Isolated SG-10: 30 mg, 35% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.43 (dd, 1H, J=12.5, 25.2 Hz), 1.73 (s, 3H), 2.15 (dd, 1H, J=12.1, 21.6 Hz), 2.26 (d, 1H, J=13.2 Hz), 2.35 (t, 1H, J=14.3 Hz), 2.61-2.64 (m, 2H), 2.74-2.78 (m, 1H), 2.85-2.90 (m, 2H), 3.41 (d, 1H, J=10.2 Hz), 3.94 (t, 1H, J=10.1 Hz), 4.91 (q, 2H, J=11.8 Hz), 5.54 (d, 1 h, J=2.0 Hz), 6.26 (d, 1H, J=2.9 Hz), 8.04 (s, 1H), 8.08 (s, 1H), 8.46 (s, 2H), 8.50 (s, 2H); ¹³C NMR (126 MHz, CDCl₃) δ=18.64, 25.71, 29.89, 30.97, 36.39, 50.21, 57.51, 68.89, 81.72, 89.91, 119.54, 121.73, 121.84, 123.90, 124.01, 126.08, 126.14, 126.18, 126.58, 126.76, 129.74, 129.90, 130.33, 131.97, 132.16, 132.24, 132.49, 133.50, 138.38, 138.56, 163.05, 163.85, 169.35; ¹⁹F NMR (376 MHz, CDCl₃): δ=−0.57 (4F); MS (ESI) calcd for C₃₃H₂₄F₁₂O₆ m/z: 744.53; found: 767.1 [M+Na]⁺, 783.1 [M+K]⁺.

SG-24: Standard procedure was applied using 14-OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 1-methylindole-3-carbonyl chloride (105 mg, 0.56 mmol), previously synthesized as described. Isolated SG-24: 28 mg, 43% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.41 (dd, 1H, J=6.5, 13.8 Hz), 1.65 (s, 3H), 2.19-2.23 (m, 2H), 2.25-2.41 (m, 1H), 2.52-2.63 (m, 1H), 2.75 (dd, 2H, J=9.8, 19.6 Hz), 2.81-2.89 (m, 2H), 3.39 (d, 1H, J=11.2 Hz), 3.78-3.86 (m, 6H), 3.95 (t, 1H, J=12.5 Hz), 4.87 (s, 2H), 5.50 (d, 1H, J=4.6 Hz), 6.22 (d, 1H, J=5.5 Hz), 7.27-7.37 (m, 6H), 7.79 (s, 1H), 7.86 (s, 1H), 8.13 (d, 1H, J=11.4 Hz), 8.23 (d, 1H, J=10.2 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=19.0, 25.9, 29.7, 31.0, 33.3 (2C), 33.4, 37.1, 50.6, 60.4, 66.5, 82.5, 87.7, 106.8, 107.9, 109.6, 109.9, 118.8 (2C), 121.5, 121.7, 122.0, 122.5, 122.8, 126.5, 126.8, 131.16, 135.4, 136.0, 137.2, 137.6, 139.3, 164.3, 164.9, 170.1; MS (ESI) calcd for C₃₅H₃₄N₂O₆ m/z: 578.67; found: 601.3 [M+Na]⁺, 617.3 [M+K]⁺, 1179.5 [2M+Na]⁺, 1195.3 [2M+K]⁺.

SG-28: Standard procedure was applied using 14-OH-MCL (30 mg, 0.11 mmol), 4-dimethylaminopyridine (14 mg, 0.11 mmol), triethylamine (74 μL, 0.56 mmol), and 2-naphthylcarbonyl chloride (105 mg, 0.56 mmol), previously synthesized as described. Isolated SG-28: 33 mg, 51% yield. ¹H NMR (500 MHz, CDCl₃): δ=1.48 (q, 1H, J=13.0 Hz), 1.74 (s, 3H), 2.15 (q, 1H, J=12.4 Hz), 2.28 (d, 1H, J=11.6 Hz), 2.39 (t, 1H, J=13.1 Hz), 2.61-2.70 (m, 1H), 2.72 (d, 1H, J=15.0 Hz), 2.86 (dd, 1H, J=6.9, 17.4 Hz), 2.89-2.93 (m, 2H), 3.43 (d, 1H, J=10.5 Hz), 4.01 (t, 1H, J=10 Hz), 4.91 (s, 2H), 5.54 (d, 1H, J=3.5 Hz), 6.27 (1H, J=4.4 Hz), 7.51-7.62 (m, 4H), 7.82-7.91 (m, 4H), 7.93 (d, 1H, J=4.2 Hz), 8.05 (d, 1H, J=3.9 Hz), 8.06-8.09 (m, 2H), 8.61 (s, 1H), 8.72 (s, 1H); ¹³C NMR (126 MHz, CDCl₃) δ=25.9, 30.0, 31.0, 36.7, 50.4, 57.9, 67.9, 82.2, 88.7, 119.1, 15.1, 125.3, 126.4, 126.7, 127.6, 127.8, 128.0, 128.2, 128.4, 128.7, 129.3, 129.6, 130.2, 130.8, 131.1, 131.4, 131.7, 132.5, 132.6, 133.4, 135.4, 135.6, 137.8, 139.1, 166.1, 166.7, 170.5; MS (ESI) calcd for C₃₇H₃₂O₆ m/z: 572.66; found: 595.2 [M+Na]⁺.

5.8 Example 8: Synthesis of C2- and C14-Substituted Micheliolide Derivatives Via Other Hydroxyl Group Functionalization Methods

This example further demonstrates the preparation of compounds of general formula I and II according to the methods provided herein. In particular, this example illustrates how C2- and C14-substituted micheliolide analogs could be prepared by coupling selective P450-catalyzed hydroxylation of the C2 or C14 site in micheliolide followed by chemical functionalization/interconversion of the enzymatically installed hydroxyl group (—OH).

Beside acylation, as shown in the Examples 4, 5, 6 and 7, other chemistries for functionalization/interconversion of a hydroxyl group can be coupled to P450-catalyzed micheliolide hydroxylation in order to obtain C2- or C14-substituted micheliolide derivatives according to the invention (Examples 8 and 9). These additional chemical methods include, but are not limited to, —OH group alkylation, oxidation, dehydration, Mitsunobu substitution, O—H carbene insertion, and deoxyhalogenation.

For example, the enzymatically produced 2(R)-hydroxy-micheliolide and 14-hydroxy-micheliolide can be converted to 2(R)-methoxy- and 14-methoxy-derivatives via alkylation with MeI in the presence of Ag₂O as a catalyst, to afford SG-39 and SG-40 (FIGS. 5 and 6 ).

The keto-derivative SG-41 in FIG. 5 was obtained via reaction of the enzymatically produced 2(R)-hydroxy-micheliolide in the presence of CrO₃ as oxidizing agent.

Tertiary alcohols, like the hydroxy substituent in position 4 of the micheliolide scaffold, can be selectively dehydrated even in the presence of a primary alcohol and/or a secondary alcohol, using appropriate acidic conditions. These studies indicate that a slightly acidic solution of p-toluenesulfonic acid in DCM is useful for the selective dehydration of the C4-hydroxy group in the chemoenzymatically produced 2(R)-hydroxy-micheliolide, thus leaving untouched the newly introduced C2-hydroxy group, to bring to the formation of SG-42 (FIG. 4 ).

Another well established method for conversion an alcohol to an ether derivative is through direct alkylation. As illustrated by SG-43, SG-44, SG-45, SG-46, SG-47 and SG-48 (FIGS. 5 and 6 ), C2- and C14-substituted micheliolide derivatives could be readily obtained via alkylation of enzymatically prepared 2- and 14-hydroxy-micheliolide with the corresponding alkyl halide in the presence of KI. These studies indicate that a variety of alkyl halides and substituted derivatives thereof can be utilized for the purpose of preparing micheliolide analogs within the scope of the invention.

The Mitsunobu reaction is a powerful tool for the transformation of primary and secondary alcohols into esters, ethers, thioethers and various other compounds. Here, the focus is on the direct transformation of the enzymatically obtained 2(R)-hydroxy-micheliolide and 14-hydroxy-micheliolide into the corresponding 2(S)-azido-micheliolide and 14-azido-micheliolide through the activation of the alcohol groups by the phosphonium intermediate generated by the interaction of TPP and DEAD. DPPA complete the reaction with the formation of 2(S)-azido-micheliolide SG-49 (FIG. 5 ), with clear inversion of configuration, and 14-hydroxy-micheliolie SG-50 (FIG. 6 ).

Another useful variant of the Mitsunobu reaction allows for the direct esterification of the enzymatically prepared 2(R)-hydroxy-micheliolide in the presence of TPP and DEAD to allow the formation of SG-51, with clear inversion of configuration at C2, as illustrated in FIG. 5 .

An established strategy for converting an alcohol to a carbamate derivative (i.e. R—OH→R—O(CO)NH—R′) involves reacting the alcohol with a desired isocyanate reagent (e.g., aryl or alkyl isocyanate compound) in the presence of DBTDL. Accordingly, as illustrated by the successful preparation of SG-56, SG-57, SG-58 and SG-59 (FIGS. 5 and 6 ), C2- and C14-carbamate derivarives of micheliolide could be readily afforded upon reaction of the enzymatically produced 2(R)-hydroxy-micheliolide (2) and 14-hydroxy-micheliolide (3), respectively, with a isocyanate reagent in the presence of CBTCL. These studies indicate that a variety of isocyanate reagents can be utilized for the purpose of preparing micheliolide analogs within the scope of the invention.

The fluorination with aminosulfuranes is a useful chemical reaction that allows the transformation of oxidized organic compounds into organofluorine compounds. Accordingly to the present invention, the chemoenzymatically introduced hydroxyl group of the 2(R)-hydroxy-micheliolide can be replaced by a fluoride through the use of DUST, with clear inversion of configuration, thus leading to 2(S)-fluoro-micheliolide SG-60 (FIG. 5 ). The same procedure can be applied on 14-hydroxy-micheliolide for the obtainment of 14-fluoro-micheliolide SG-61, as shown in FIG. 6 .

General Conditions for the Alkylation (Methylation) of 2(R)-Hydroxy-Micheliolide and 14-Hydroxy-Micheliolide:

To a stirred solution of 2(R)—OH-MCL or 14-OH-MCL (0.02 mmol) in dry DMF at r.t. an excess of Ag₂O (0.1 mmol) was added and the reaction mixture was stirred 10 min at r.t. MeI (0.1 mmol) was then added and the reaction was warmed to 50° C. After 24 h, the TLC showed the formation of a new product. Few drops of H₂O were added to quench the reaction mixture and then Ag₂O was filtered away. The remaining organic solvent was evaporated at Hi-Vacuum and the obtained crude product was purified by flash chromatography on silica gel (eluting mixture EtOAc 50% in n-Hexane).

General Conditions for the Oxidation of 2(R)-Hydroxy-Micheliolide:

CrO₃ (0.9 mmol) was added portion wise to H₂O (105 μL) and the resulting solution cooled at 0° C. Conc. H₂SO₄ (30 μL) was added dropwise and the solution stirred for 15 min. The resulting red solution was added dropwise to a solution of 2(R)—OH-MCL (0.11 mmol) in Acetone (750 μL) at 0° C. and stirred for 1 h. H₂O (2 mL) and Et₂O (2 mL) were added, the phases were separated and the organic layer was concentrated and purified by flash chromatography on silica gel (eluting mixture EtOAc 30% in n-Hexane).

General Conditions for the Dehydration of Position C₄-C₅ of 2(R)-Hydroxy-Micheliolide:

p-toluene-sulfonic acid (0.22 mmol) was added to a solution of 2(R)—OH-MCL (0.11 mmol) in anhydrous DCM (2 mL) at r.t. and stirred for 12 h.; H₂O (5 mL) was added to the reaction mixture and the aqueous phase was extracted with EtOAc (3×). The collected organic fractions were dried in vacuo and the crude product was purified by flash chromatography on silica gel (eluting mixture EtOAc 20% in n-Hexane).

General Conditions for the Direct Alkylation of 2(R)- and 14-Hydroxy-Micheliolide:

2(R)—OH-MCL or 14-OH-MCL (0.04 mmol) were dissolved in anhydrous DMF (1 mL) under a Ar atmosphere, then anhydrous K₂CO₃ (0.07 mmol) and a catalytic amount of KI were added, followed by benzyl bromide (0.04 mmol). The reaction was stirred at r.t. 12 h. The solvent was then evaporated and the residue taken up in NaHCO₃ saturated solution and extracted with EtOAc (3×). The collected organic phases ware dried over Na₂SO₄ and the solvent was removed in vacuo. The resulting crude product was purified by flash chromatography on silica gel (eluting mixture 50% EtOAc in n-Hexane).

General Conditions for the Azido Group Introduction into 2(R)- and 14-Hydroxy-Micheliolide Through Mitsunobu Reaction:

To a solution of 2(R)—OH-MCL or 14-OH-MCL (0.04 mmol), TPP (0.08 mmol) and DPPA (0.08 mmol) in anhydrous THF cooled at 0° C. under Ar atmosphere DEAD (0.08 mmol) was added dropwise. The reaction was warmed at r.t. and stirred 12 h. Disappearance of the starting material on TLC indicates the completion of the reaction. The reaction mixture was evaporated and the crude was purified by flash chromatography on silica gel (eluting mixture 40% EtOAc in n-Hexane).

General Conditions for the Mitsunobu Esterification of 2(R)-Hydroxy-Micheliolide:

To a solution of 2(R)—OH-MCL (0.04 mmol), TPP (0.16 mmol) and benzoic acid (0.17 mmol) in anhydrous THF cooled at 0° C. under Ar atmosphere DEAD (0.16 mmol) was added dropwise. The reaction was warmed at r.t. and stirred for 12 h. NaHCO₃ saturated solution was added to the reaction mixture and the aqueous phase was extracted with DCM (2×); the collected organic phases were dried over Na₂SO₄, concentrated in vacuo and the crude product was purified by flash chromatography on silica gel (eluting mixture EtOAc 20% in n-Hexane).

General Conditions for Carbamate Derivatization of 2(R)-Hydroxy-Micheliolide and 14-Hydroxy-Micheliolide:

To a solution of 2(R)—OH-MCL or 14-OH-MCL (0.05 mmol), and the appropriate isocyanate (0.07 mmol) in anhydrous DCM (2 mL) under Ar atmosphere DBTDL (dibuthyltin dilaurate) (20% mol) was added and the reaction was stirred at r.t. 12 h. The disappearance of the SM on TLC indicated the completion of the reaction. A saturated solution of NaHCO₃ was added and the aqueous phase was extracted with DCM (3×). The collected organic layers were dried over Na₂SO₄, concentrated in vacuo and the crude product was purified by flash chromatography on silica gel (eluting mixture EtOAc 50% in n-Hexane).

General Conditions for the Fluorination of 2(R)- and 14-Hydroxy-Micheliolide:DAST (0.22 mmol) was added dropwise to a solution of 2(R)—OH-MCL or 14-OH-MCL in anhydrous DCM (2 mL) under Ar atmosphere cooled at −78° C. The reaction was warmed to 0° C. and stirred until total disappearance of the SM was observed in TLC. The reaction was added of a saturated solution of NaHCO₃ and extracted with DCM (3×). The collected organic fractions were dried over Na₂SO₄, concentrated in vacuo and the crude product was purified by flash chromatography on silica gel (eluting mixture EtOAc 25% in n-Hexane).

SG-39: standard procedure was applied using 2(R)—OH-MCL (5 mg, 0.02 mmol), Ag₂O (23 mg, 0.1 mmol) and MeI (7 mL, 0.1 mmol) to obtain the desired product as a colorless oil (0.6 mg, 12% yield); ¹H NMR (500 MHz, CDCl₃): δ=0.88-0.92 (m, 1H), 1.09 (s, 3H), 1.50 (s, 3H), 1.72-1.88 (m, 2H), 2.10-2.19 (m, 1H), 2.32-2.42 (m, 1H), 2.51 (d, 1H, J=8.5 Hz), 2.55-2.66 (m, 1H), 2.71 (t, 1H, J=9.0 Hz), 2.82 (d, 1H, J=8.0 Hz), 3.79 (s, 3H), 3.80-3.88 (m, 1H), 4.60 (s, 1H), 5.52 (d, 1H, J=3.0 Hz), 6.22 (d, 1H, J=3.0 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=19.9, 26.4, 27.2, 37.8, 49.5, 50.6, 58.2, 58.9, 79.7, 80.0, 85.3, 119.7, 125.8, 134.2, 140.9, 170.4; MS (ESI) calcd for C₁₆H₂₂O₄ m/z: 278.35; found: 301.2 [M+Na]⁺, 579.5 [2M+Na]⁺.

SG-40: standard procedure was applied using 14-OH-MCL (5 mg, 0.02 mmol), Ag₂O (23 mg, 0.1 mmol) and MeI (7 mL, 0.1 mmol) to obtain the desired compound as a colorless oil (1.2 mg, 23% yield); ¹H NMR (500 MHz, CDCl₃): δ=1.25-1.38 (m, 4H), 1.54 (t, 1H, J=9.0 Hz), 1.79-1.85 (m, 3H), 2.10-2.16 (m, 2H), 2.30-2.35 (m, 1H), 2.52-2.62 (m, 2H), 2.70 (t, 1H, J=9.0 Hz), 2.82 (d, 1H, J=10.5 Hz), 3.30 (s, 3H), 3.85 (s, 2H), 5.52 (d, 1H, J=3.0 Hz), 6.22 (d, 1H, J=3.0 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=22.8, 25.7, 29.7, 30.6, 38.3, 50.2, 57.9, 58.8, 76.2, 80.3, 84.2, 119.7, 132.2, 137.9, 139.1, 169.9; MS (ESI) calcd for C₁₆H₂₂O₄ m/z: 278.35; found: 301.3 [M+Na]⁺, 317.2 [M+K]⁺, 579.3 [2M+Na]⁺.

SG-41: standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol), CrO₃ (90 mg, 0.9 mmol) in H₂O (105 μL) and conc. H₂SO₄ (30 μL) to obtain the desired product as a colorless oil (7 mg, 24% yield); ¹H NMR (500 MHz, CDCl₃): C=1.42-1.50 (m, 1H), 1.61 (s, 3H), 2.03-2.17 (m, 2H), 2.18 (s, 3H), 2.28-2.37 (m, 1H), 2.49 (br s, 1H), 2.52-2.64 (m, 1H), 2.70 (s, 1H, J=5.5 Hz), 2.85-2.97 (m, 1H), 3.02 (dd, 1H, J₁=10.0 Hz, J₂=2.5 Hz), 4.43 (t, 1H, J=11.0 Hz), 5.54 (d, 1H, J=3.0 Hz), 6.26 (d, 1H, J=3.0 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 20.4, 24.6, 25.8, 35.4, 48.5, 49.8, 71.8, 77.3, 82.5, 119.6, 126.3, 138.3, 163.5, 170.2, 207.0; MS (ESI) calcd for C₁₅H₁₈O₄ m/z: 262.31; found: 263.4 [M+H]⁺, 285.3 [M+Na]⁺, 547.2 [2M+Na]⁺.

SG-42: standard procedure was applied using 2(R)—OH-MCL (30 mg, 0.11 mmol) and p-toluene-sulfonic acid (19 mg, 0.22 mmol) to obtain the desired product as a yellow solid (6 mg, 32% yield); ¹H NMR (500 MHz, CDCl₃): δ=1.34-1.48 (m, 1H), 1.39 (s, 3H), 1.93 (s, 3H), 2.11 (t, 1H, J=14.0 Hz), 2.32-2.40 (m, 2H), 2.41 (br s, 1H), 2.68-2.76 (m, 2H), 2.84 (t, 1H, J=8.5 Hz), 4.15 (t, 1H, J=9.5 Hz), 5.55 (d, 1H, J=6.5 Hz), 5.92 (s, 1H), 6.25 (d, 1H, J=3.5 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 20.1, 21.6, 25.8, 35.4, 42.9, 52.8, 69.8, 79.5, 119.8, 123.3, 124.6, 128.4, 139.5, 160.2, 170.6; MS (ESI) calcd for C₁₅H₁₈O₃ m/z: 246.31; found: 247.3 [M+H]⁺, 263.3 [M+Na]⁺, 285.3 [M+K]⁺, 493.3 [2M+H]⁺, 515.3 [2M+Na]⁺.

SG-43: standard procedure was applied using 2(R)—OH-MCL (10 mg, 0.04 mmol), K₂CO₃ (11 mg, 0.07 mmol), a catalytic amount of KI and benzyl bromide (5 μL, 0.04 mmol) to obtain the desired product as a colorless oil (4 mg, 30% yield). ¹H NMR (500 MHz, CDCl₃): C=1.23 (s, 3H), 1.26-1.48 (m, 1H), 1.61 (s, 3H), 2.00 (t, 1H, J=9.5 Hz), 2.15 (d, 1H, J=10.5 Hz), 2.17-2.42 (m, 3H), 2.57 (t, 1H, J=9.5 Hz), 2.74 (t, 1H, J=8.0 Hz), 3.08 (d, 1H, J=7.5 Hz), 3.85 (t, 1H, J=10.5 Hz), 4.68 (s, 2H), 5.02 (d, 1H, J=5.5 Hz), 5.76 (t, 1H, J=8.0 Hz), 6.25 (d, 1H, J=5.0 Hz), 7.42 (t, 2H, J=8.0 Hz), 7.61 (t, 1H, J=7.5 Hz), 7.71 (d, 2H, J=9.5 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 22.5, 25.6, 29.2, 38.1, 50.3, 58.8, 62.6, 75.2, 80.3, 81.8, 83.7, 119.8, 124.3, 128.6 (2C), 129.2 (2C), 130.0, 133.1, 138.9, 140.4, 169.8; MS (ESI) calcd for C₂₂H₂₆O₄ m/z: 354.4; found: 377.5 [M+Na]⁺, 393.3 [M+K]⁺.

SG-44: standard procedure was applied using 14-OH-MCL (20 mg, 0.08 mmol), K₂CO₃ (22 mg, 0.14 mmol), a catalytic amount of KI and benzyl bromide (10 μL, 0.08 mmol) to obtain the desired compound as a colorless oil (10 mg, 38% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.35-1.37 (m, 1H), 1.36 (s, 3H), 1.82-1.90 (m, 2H), 2.18 (d, 1H, J=13.5 Hz), 2.29 (t, 1H, J=15 Hz), 2.39-2.50 (m, 2H), 2.60 (d, 1H, J=13 Hz), 2.62-2.74 (m, 2H), 2.86 (d, 1H, J=10.5 Hz), 3.85 (t, 1H, J=10.5 Hz), 4.05 (s, 2H), 4.50 (s, 2H), 5.52 (d, 1H, J=3.0 Hz), 6.23 (d, 1H, J=3.0 Hz), 7.38 (d, 2H, J=8.0 Hz), 7.48 (t, 2H, J=7.5 Hz), 7.52 (t, 1H, J=7.0 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 22.8, 25.7, 29.3, 30.8, 38.2, 50.0, 58.9, 67.6, 69.2, 80.1, 83.6, 119.7, 127.5, 128.4, 129.5, 133.1, 137.2, 138.5, 140.0, 169.4; MS (ESI) calcd for C₂₂H₂₆O₄ m/z: 354.4; found: 393.3 [M+K]⁺.

SG-45: standard procedure was applied using 2(R)—OH-MCL (10 mg, 0.04 mmol), K₂CO₃ (11 mg, 0.07 mmol), a catalytic amount of KI and 2,4-di-fluorobenzyl bromide (6 μL, 0.04 mmol) to obtain the desired product as a colorless oil (6 mg, 46% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.38 (s, 3H), 1.41-1.45 (m, 1H), 1.74 (s, 3H), 2.06 (dd, 1H, J₁=8.0 Hz, J₂=3.0 Hz), 2.15 (d, 1H, J=10.0 Hz), 2.34 (s, 2H), 2.63 (dd, 2H, J₁=8.0 Hz, J₂=3.5 Hz), 2.74 (t, 1H, J=10.0 Hz), 3.06 (d, 1H, J=9.5 Hz), 3.85 (t, 1H, J=9.8 Hz), 4.60 (s, 2H), 5.55 (d, 1H, J=3.5 Hz), 5.88 (t, 1H, J=7.0 Hz), 6.26 (d, 1H, J=3.5 Hz), 7.83 (d, 1H, J=8.0 Hz), 7.88 (d, 1H, J=8.0 Hz), 7.99 (s, 1H); ¹³C NMR (126 MHz, CDCl₃) δ 24.1, 24.2, 25.8, 35.6, 45.1, 48.2, 58.1, 65.6, 75.7, 83.8, 86.2, 120.4, 124.0 (d, J=21.4 Hz), 128.7, 129.6 (d, J=37.8 Hz), 130.2, 130.4, 133.3 (d, J=34.2 Hz), 134.6, 138.1, 139.6, 169.2; ¹⁹F NMR (376 MHz, CDCl₃): δ −0.86, 2.90; MS (ESI) calcd for C₂₄H₂₄F₂O₄ m/z: 390.43; found: 413.4 [M+Na]⁺, 803.4 [2M+Na]⁺.

SG-46: standard procedure was applied using 14-OH-MCL (20 mg, 0.08 mmol), K₂CO₃ (22 mg, 0.14 mmol), a catalytic amount of KI and 2,4-di-fluorobenzyl bromide (13 μL, 0.08 mmol) to obtain the desired compound as a colorless oil (15 mg, 53% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.28-1.36 (m, 4H), 1.84-1.36 (m, 2H), 2.16 (d, 1H, J=13.2 Hz), 2.27 (t, 1H, J=14.5 Hz), 2.39-2.50 (m, 1H), 2.53 (d, 1H, J=16.0 Hz), 2.63-2.73 (m, 3H), 2.85 (d, 1H, J=10.0 Hz), 3.83 (t, 1H, J=10.5 Hz), 4.46 (dd, 2H, J₁=15.0 Hz, J₂=8.0 Hz), 4.78 (s, 2H), 5.51 (d, 1H, J=1.5 Hz), 6.23 (d, 1H, J=2.0 Hz), 7.89 (s, 1H), 7.99 (s, 2H); ¹³C NMR (126 MHz, CDCl₃) δ 22.7, 25.6, 29.3, 31.3, 38.1, 49.8, 59.0, 64.3, 69.6, 80.0, 83.5, 86.2, 119.4, 123.5, 127.9, 128.2, 131.4, 132.7, 134.5, 138.2, 142.6, 169.2; ¹⁹F NMR (376 MHz, CDCl₃): δ −0.86, 2.72; MS (ESI) calcd for C₂₄H₂₄F₂O₄ m/z: 390.43; found: 413.4 [M+Na]⁺, 803.4 [2M+Na]⁺.

SG-47: standard procedure was applied using 2(R)—OH-MCL (10 mg, 0.04 mmol), K₂CO₃ (11 mg, 0.07 mmol), a catalytic amount of KI and 4-CF₃-benzyl bromide (7 μL, 0.04 mmol) to obtain the desired product as a colorless oil (4 mg, 25% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.35 (s, 3H), 1.38-1.48 (m, 1H), 1.70 (s, 3H), 2.01 (dd, 1H, J₁=12.5 Hz, J₂=4.5 Hz), 2.18 (d, 1H, J=11.5 Hz), 2.34-2.42 (m, 3H), 2.60 (t, 1H, J=8.0 Hz), 2.78 (t, 1H, J=9.5 Hz), 3.11 (d, 1H, J=8.0 Hz), 3.86 (t, 1H, J=10.0 Hz), 4.61 (s, 2H), 5.56 (d, 1H, J=2.5 Hz), 5.84 (t, 1H, J=7.5 Hz), 6.27 (d, 1H, J=3.0 Hz), 7.70 (d, 2H, J=8.0 Hz), 8.14 (d, 2H, J=8.0 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 24.1, 24.2, 25.7, 35.7, 45.5, 48.5, 58.2, 74.5, 80.2, 82.8, 83.9, 120.3, 125.4, 130.0 (4C), 130.8, 132.6 (d, J=113.4 Hz), 134.6 (d, J=32.3 Hz), 138.2, 139.1, 169.3; ¹⁹F NMR (376 MHz, CDCl₃): δ −0.72; MS (ESI) calcd for C₂₃H₂₅F₃O₄ m/z: 424.44; found: 445.3 [M+Na]⁺.

SG-48: standard procedure was applied using 14-OH-MCL (20 mg, 0.08 mmol), K₂CO₃ (22 mg, 0.14 mmol), a catalytic amount of KI and 4-CF₃-benzyl bromide (14 μL, 0.08 mmol) to obtain the desired compound as a colorless oil (10 mg, 41% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.32-1.39 (m, 4H), 1.83-1.90 (m, 2H), 2.19 (d, 1H, J=13.5 Hz), 2.27 (t, 1H, J=13.5 Hz), 2.45 (t, 1H, J=4.0 Hz), 2.58 (d, 1H, J=16.5 Hz), 2.68-2.75 (m, 3H), 2.86 (d, 1H, J=10.5 Hz), 3.87 (t, 1H, J=10.5 Hz), 4.68 (s, 2H), 5.01 (s, 2H), 5.51 (d, 1H, J=2.5 Hz), 6.22 (d, 1H, J=3.0 Hz), 7.71 (d, 2H, J=8.0 Hz), 8.14 (d, 2H, J=8.0 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 22.8, 25.4, 29.4, 30.8, 38.2, 50.0, 59.0, 68.2, 71.2, 80.1, 83.5, 119.7, 125.4 (t, J=97.5 Hz), 129.5 (2C), 130.0 (2C), 134.4 (t, J=102.4 Hz), 138.4 (2C), 140.6 (2C), 169.3; ¹⁹F NMR (376 MHz, CDCl₃): δ −0.73; MS (ESI) calcd for C₂₃H₂₅F₃O₄ m/z: 424.44; found: 445.3 [M+Na]⁺.

SG-49: standard procedure was applied using 2(R)—OH-MCL (10 mg, 0.04 mmol), TPP (20 mg, 0.08 mmol), DPPA (16 μL, 0.08 mmol) and DEAD (12 μL, 0.08 mmol) to obtain the desired product as a colorless oil (2 mg, 13% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.30-1.38 (m, 4H), 1.82-1.70 (m, 2H), 2.18 (d, 1H, J=9.5 Hz), 2.27-2.41 (m, 2H), 2.48 (d, 1H, J=8.5 Hz), 2.54 (dd, 1H, J₁=18.0 Hz, J₂=4.2 Hz), 2.71 (t, 1H, J=9.5 Hz), 2.85 (d, 1H, J=10.0 Hz), 3.80-3.95 (m, 2H), 5.53 (d, 1H, J=3.0 Hz), 5.22 (t, 1H, J=7.5 Hz), 6.22 (d, 1H, J=5.0 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 23.5, 29.7, 32.1, 35.7, 51.8, 56.1, 59.8, 65.5, 80.0, 82.6, 121.8, 125.3, 138.8, 139.8, 169.3; MS (ESI) calcd for C₁₅H₁₉N₃O₄ m/z: 289.34; found: 290.2 [M+H]⁺, 312.2 [M+Na]⁺, 328.2 [M+K]⁺, 579.3 [2M+H]⁺, 601.3 [2M+K]⁺.

SG-50: standard procedure was applied using 14-OH-MCL (20 mg, 0.08 mmol), TPP (40 mg, 0.16 mmol), DPPA (32 μL, 0.16 mmol) and DEAD (24 μL, 0.16 mmol) to obtain the desired compound as a colorless oil (15 mg, 68% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.30-1.39 (m, 4H), 1.84-1.90 (m, 2H), 2.17 (d, 1H, J=8.5 Hz), 2.28-2.39 (m, 2H), 2.47 (d, 1H, J=12.5 Hz), 2.51-2.57 (m, 1H), 2.73 (t, 1H, J=7.5 Hz), 2.86 (d, 1H, J=8.0 Hz), 3.82-3.89 (m, 2H), 4.21 (q, 1H, J=8.0 Hz), 5.51 (d, 1H, J=3.0 Hz), 6.23 (d, 1H, J=3.0 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 22.6, 25.5, 29.7, 32.1, 38.1, 49.8, 56.1, 58.8, 80.0, 83.6, 119.8, 129.3, 138.3, 140.1, 169.3; MS (ESI) calcd for C₁₅H₁₉N₃O₄ m/z: 289.34; found: 290.2 [M+H]⁺, 312.2 [M+Na]⁺, 328.2 [M+K]⁺, 579.3 [2M+H]⁺, 601.3 [2M+K]⁺.

SG-51: standard procedure was applied using 2(R)—OH-MCL MCL (10 mg, 0.04 mmol), TPP (40 mg, 0.16 mmol) benzoic acid (19 μL, 0.17 mmol) and DEAD (24 μL, 0.16 mmol) to obtain the desired product as a colorless oil (10 mg, 36% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.21 (s, 3H), 1.30-1.48 (m, 1H), 1.70 (s, 3H), 2.00 (dd, 1H, J₁=9.5 Hz, J₂=3.0 Hz), 2.18 (d, 1H, J=10.5 Hz), 2.34-2.42 (m, 3H), 2.60 (t, 1H, J=7.5 Hz), 2.78 (t, 1H, J=7.0 Hz), 3.10 (d, 1H, J=4.5 Hz), 3.85 (t, 1H, J=10.5 Hz), 5.51 (d, 1H, J=3.0 Hz), 5.84 (t, 1H, J=7.5 Hz), 6.23 (d, 1H, J=3.0 Hz), 7.45 (t, 2H, J=8.0 Hz), 7.57 (t, 1H, J=7.5 Hz), 8.03 (d, 2H, J=7.5 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 22.8, 25.4, 25.7, 38.2, 45.5, 50.0, 58.9, 74.5, 83.6, 119.7, 128.4 (2C), 129.5 (2C), 130.0, 133.1, 138.5 (2C), 140.0 (2C), 166.5, 169.4; MS (ESI) calcd for C₂₂H₂₄O₅ m/z: 368.43; found: 391.3 [M+Na]⁺, 759.3 [2M+Na]⁺.

SG-56: standard procedure was applied using 2(R)—OH-MCL MCL (12 mg, 0.05 mmol), phenyl isocyanate (8 μL, 0.07 mmol) and DBTDL (20% mol) to obtain the desired product as a white solid (10 mg, 86% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.25-1.34 (m, 4H), 1.77 (s, 3H), 2.00 (dd, 1H, J₁=12.5, J₂=4.0 Hz), 2.15 (d, 1H, J=12.0 Hz), 2.32-2.35 (m, 3H), 2.50 (dd, 1H, J₁=12.5 Hz, J₂=5.0 Hz), 2.73 (t, 1H, J=10.0 Hz), 3.02 (d, 1H, J=9.0 Hz), 3.83 (t, 1H, J=10.0 Hz), 5.55 (d, 1H, J=3.0 Hz), 5.64 (t, 1H, J=7.5 Hz), 6.26 (d, 1H, J=3.0 Hz), 6.66 (s, 1H, NH), 7.06 (t, 1H, J=7.0 Hz), 7.30 (t, 2H, J=7.5 Hz), 7.36-7.38 (m, 2H); ¹³C NMR (126 MHz, CDCl₃) δ 24.2, 24.7, 25.8, 29.3, 35.7, 45.7, 48.5, 58.2, 74.0, 83.9, 118.5, 120.2, 123.5, 129.1 (4C), 131.0, 137.7, 138.3, 139.0, 169.3; MS (ESI) calcd for C₂₂H₂₅NO₅ m/z: 383.44; found: 406.3 [M+Na]⁺, 789.4 [2M+Na]⁺.

SG-57: standard procedure was applied using 14-OH-MCL (24 mg, 0.10 mmol), phenyl isocyanate (16 μL, 0.14 mmol) and DBTDL (20% mol) to obtain the desired compound as a white solid (20 mg, 87% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.34 (s, 3H), 1.60-1.68 (m, 1H), 1.78-1.90 (m, 2H), 2.14-2.24 (m, 2H), 2.33 (d, 1H, J=7.5 Hz), 2.37-2.43 (m, 1H), 2.53 (d, 1H, J=16.0 Hz), 2.62-2.72 (m, 2H), 2.83 (d, 1H, J=10.5 Hz), 3.83 (t, 1H, J=10.5 Hz), 4.62 (s, 2H), 5.51 (s, 1H), 6.22 (d, 1H, J=3.5 Hz), 6.73 (br. s, 1H, NH), 7.06 (t, 1H, J=7.0 Hz), 7.30 (t, 2H, J=8.0 Hz), 7.36-7.39 (m, 2H); ¹³C NMR (126 MHz, CDCl₃) δ 22.6, 25.6, 29.2, 30.8, 38.2, 50.0, 58.9, 67.9, 80.1, 83.6, 118.6, 119.7, 123.6, 129.1 (4C), 130.0, 137.7, 138.4, 140.1, 169.5; MS (ESI) calcd for C₂₂H₂₅NO₅ m/z: 383.44; found: 406.3 [M+Na]⁺, 789.4 [2M+Na]⁺.

SG-58: standard procedure was applied using 2(R)—OH-MCL (12 mg, 0.05 mmol), 4-CF₃-phenyl isocyanate (10 μL, 0.07 mmol) and DBTDL (20% mol) to obtain the desired product as a white solid (14 mg, 90% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.29 (s, 3H), 1.45-1.51 (m, 1H), 1.77 (s, 3H), 2.01 (dd, 1H, J₁=13.0 Hz, J₂=4.5 Hz), 2.16 (dd, 1H, J₁=14.0 Hz, J₂=2.5 Hz), 2.35 (s, 2H), 2.51 (dd, 1H, J₁=13.0 Hz, J₂=5.0 Hz), 2.73 (t, 1H, J=9.0 Hz), 3.02 (d, 1H, J=10.0 Hz), 3.84 (t, 1H, J=10.0 Hz), 5.55 (d, 1H, J=3.0 Hz), 5.65 (t, 1H, J=7.5 Hz), 6.26 (d, 1H, J=3.5 Hz), 6.86 (s, 1H, NH), 7.50 (d, 2H, J=8.5 Hz), 7.56 (d, 2H, J=8.5 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 24.1, 24.2, 25.7, 35.7, 45.7, 48.5, 58.2, 74.5, 83.8, 116.1, 118.0 (2C), 120.3, 123.0, 126.3 (2C), 130.8, 133.6, 138.2, 139.3, 140.9, 152.6, 169.2; ¹⁹F NMR (376 MHz, CDCl₃): δ 0.37; MS (ESI) calcd for C₂₃H₂₄F₃NO₅ m/z: 451.44; found: 475.4 [M+Na]⁺, 925.6 [2M+Na]⁺.

SG-59: standard procedure was applied using 14-OH-MCL (24 mg, 0.10 mmol), 4-CF₃-phenyl isocyanate (20 μL, 0.14 mmol) and DBTDL (20% mol) to obtain the desired compound as a white solid (29 mg, 93% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.32-1.39 (m, 4H), 1.83-1.90 (m, 2H), 215-2.25 (m, 2H), 2.36-2.41 (m, 1H), 2.52 (d, 1H, J=16.0 Hz), 2.63-2.72 (m, 2H), 2.83 (d, 1H, J=10.5 Hz), 3.83 (t, 1H, J=10.0 Hz), 4.64 (s, 2H), 5.51 (d, 1H, J=2.5 Hz), 6.22 (d, 1H, J=3.0 Hz), 6.94 (s, 1H, NH), 7.50 (d, 2H, J=8.5 Hz), 7.55 (d, 2H, J=8.5 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 22.8, 25.6, 29.9, 30.9, 38.2, 49.9, 58.9, 68.2, 80.1, 83.6, 118.0 (2C), 119.8, 123.0, 125.3 (J=138.5 Hz), 126.3 (2C), 129.7, 138.4, 140.5, 140.9, 153.1, 169.4; ¹⁹F NMR (376 MHz, CDCl₃): δ 0.36; MS (ESI) calcd for C₂₃H₂₄F₃NO₅ m/z: 451.44; found: 475.4 [M+Na]⁺, 925.6 [2M+Na]⁺.

SG-60: standard procedure was applied using 2(R)—OH-MCL (10 mg, 0.04 mmol) and DAST (15 μL, 0.22 mmol) to obtain the desired product as a colorless oil (3 mg, 29% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.21-1.34 (m, 4H), 1.36-1.42 (m, 1H), 1.51-1.58 (m, 1H), 1.83 (dd, 1H, J₁=8.4 Hz, J₂=3.0 Hz), 1.95-2.06 (m, 1H), 2.24-2.31 (m, 3H), 2.39 (d, 1H, J=14.0 Hz), 2.61-2.70 (m, 2H), 2.937 (t, 1H, J=7.5 Hz), 5.11 (d, 1H, J=3.5 Hz), 5.55 (d, 1H, J=3.0 Hz), 6.25 (d, 1H, J=3.0 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 22.8, 30.5, 31.5, 33.2 (d, J=54.3 Hz), 37.7, 46.5, 64.5 (d, J=60.2 Hz), 79.6, 82.4, 115.4, 121.1, 123.7, 124.0, 137.6, 168.2; ¹⁹F NMR (376 MHz, CDCl₃): δ −179. 6; MS (ESI) calcd for C₁₅H₁₉FO₃ m/z: 266.31; found: 289.2 [M+Na]⁺, 555.3 [2M+Na]⁺.

SG-61: standard procedure was applied using 14-OH-MCL (20 mg, 0.08 mmol) and DAST (30 μL, 0.44 mmol) to obtain the desired compound as a colorless oil (8 mg, 41% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.23-1.39 (m, 4H), 1.78-1.90 (m, 2H), 2.12-2.24 (m, 2H), 2.34 (br. s, 1H), 2.50-2.54 (m, 1H), 2.61 (d, 1H, J=13.5 Hz), 2.72 (t, 1H, J=9.5 Hz), 2.84 (t, 1H, J=9.0 Hz), 3.83 (t, 1H, J=9.0 Hz), 4.82 (d, 2H, J=47.5 Hz), 5.53 (d, 1H, J=3.0 Hz), 6.23 (d, 1H, J=3.0 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 22.7, 25.6, 28.9, 29.8, 38.1, 49.9, 59.0, 79.9, 83.7 (d, J=54.5), 85.2, 119.8, 130.8, 138.4, 140.1, 147.3, 169.4; ¹⁹F NMR (376 MHz, CDCl₃): δ −217. 3; MS (ESI) calcd for C₁₅H₁₉FO₃ m/z: 266.31; found: 289.2 [M+Na]⁺, 555.3 [2M+Na]⁺.

5.9 Example 9: Synthesis of C2- and C14-Substituted Micheliolide Derivatives Via Successive Transformations of the Previously Inserted Functional Groups

This example describes and demonstrates the preparation of compounds of general formula I and II according to the methods provided herein. In particular, it demonstrates how C2- and C14-substituted micheliolide analogs, coming from the enzymatic insertion of the hydroxyl group followed by chemical transformation of the same, could be further functionalized by reacting the functional groups already in place at the C2 or C14 site in micheliolide, thus gaining the access to a number of totally different micheliolide derivatives.

According to the present invention, the azido group (—N₃) can be further functionalized thanks to the enormous versatility of the same: the Huisgen reaction, the aza-Wittig reaction, the Sundberg cyclization, the Boyer and Boyer-Aubé rearrangements, the Curtius rearrangement, are only some of the organic reactions that can be performed starting from a primary or secondary azide. In particular, the present invention focus on the cycloaddition with an alkyne to generate a triazole derivative, or the direct reduction to amine (—NH₂) followed by amide formation through the coupling with a (hetero)aromatic or aliphatic carboxylic acid (FIGS. 5 and 6 ).

An established strategy for the synthesis of triazole-containing compounds is the cycloaddition of primary or secondary azides with alkynes. In the present invention, the chemoenzymatically-derived 2(S)-azido-micheliolide and 14-azido-micheliolide were reacted with (substituted)phenylacetylene in the presence of copper sulfate and sodium ascorbate to get SG-52 and SG-53 (FIGS. 5 and 6 ).

The Staudinger reaction is a well-known procedure for the direct reduction of azides to the corresponding amines, therefore capable of increasing the amount of applicable chemistry on azide-containing compounds. The chemoenzymatically-obtained 2(S)-azido-micheliolide and 14-azido-micheliolide can be reduced to the corresponding amine-containing derivatives in the presence of TPP to allow the formation of SG-54 and SG-55 (FIGS. 5 and 6 ), two excellent starting point for further functionalization of the micheliolide scaffolds.

A useful chemical transformation of amine-containing compounds is the coupling with a carboxylic acid, whereas the acidic function can contain an aliphatic, an aromatic or an aminoacidic group, in order to form an amide bond. The huge variety of coupling agents available nowadays allows for the reaction between a great number of different amines and carboxylic acids. The present invention provides the method for the obtainment of amide-containing micheliolide derivative SG-62, as illustrated in FIG. 6 , starting from 14-amino-micheliolide, DCC and Et₃N.

General conditions for the cycloaddition of 2(S)-azido-micheliolide and 14-azido-micheliolide: to a solution of 2(S)-azido-MCL or 14-azido-MCL (0.04 mmol) and phenylacetylene (0.06 mmol) in a 1:1 DCM/H₂O mixture, copper sulfate pentahydrate (0.06 mmol) and sodium ascorbate (0.26 mmol) were added at r.t. The reaction was stirred for 12 h followed by extraction wit DCM (3×). The combined organic solvents were dried over Na₂SO₄, concentrated in vacuo and purified by flash chromatography on silica gel (eluting mixture EtOAc 100%).

General conditions for the Staudinger reduction of 2(S)-azido-micheliolide and 14-azido-micheliolide: a solution of 2(S)-azido-MCL or 14-azido-MCL (0.06 mmol) and TPP (0.06 mmol) in dry THF was stirred at r.t. for 6 h and then warmed up at 45° C. for 12 h. Disappearance of the starting material indicated the completion of the reaction. A saturated solution of NaHCO₃ was added to the reaction mixture and the aqueous phase was extracted with EtOAc (3×). The combined organic phases were dried over Na₂SO₄, evaporated in vacuo and the crude product was purified by flash chromatography on silica gel (eluting mixture MeOH 5% in EtOAc).

General conditions for the coupling reaction of 14-NH₂-micheliolide: DCC (0.06 mmol) and triethylamine (0.06 mmol) were added to a solution of 14-NH₂-MCL (0.03 mmol) in anhydrous DMF cooled to 0° C. and the mixture was stirred 1 h at 0° C.; a solution of benzyl alcohol (0.06 mmol) and triethylamine (0.06 mmol) in anhydrous DMF was added to the previous reaction mixture. The solution was allowed to warm up to r.t. and stirred 12 h. The reaction was directly concentrated in vacuo and the crude product was purified by flash chromatography on silica gel (eluting mixture EtOAc 20% in n-Hexane).

SG-52: standard procedure was applied using 2(S)-azido-MCL (10 mg, 0.04 mmol), phenylacetylene (6 μL, 0.06 mmol) in a 1:1 DCM/H₂O mixture (3 mL), copper sulfate pentahydrate (13 mg, 0.06 mmol) and sodium ascorbate (52 mg, 0.26 mmol) to obtain the desired product as a colorless oil (3 mg, 23% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.34-1.42 (m, 4H), 1.89-1.97 (m, 3H), 2.04-2.16 (m, 3H), 2.34 (d, 1H, J=11.0 Hz), 2.49-2.58 (m, 1H), 2.69 (t, 1H, J=4.5 Hz), 2.75-2.79 (m, 1H), 2.90 (d, 1H, J=10.5 Hz), 3.88 (t, 1H, J=8.0 Hz), 4.98 (d, 1H, J=3.0 Hz), 5.18 (d, 1H, J=7.0 Hz), 6.21 (d, 1H, J=3.5 Hz), 7.34-7.44 (m, 3H), 7.66 (s, 1H), 7.83 (d, 2H, J=7.5 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 22.9, 29.9, 30.7, 38.7, 49.8, 55.0, 59.0, 59.9, 65.4, 80.1, 81.3, 119.1, 120.0, 125.7, 128.2, 128.3, 128.8, 128.9, 130.3, 138.0, 140.8, 148.2, 169.2; MS (ESI) calcd for C₂₃H₂₅N₃O₃ m/z: 391.47; found: 392.3 [M+H]⁺, 414.3 [M+Na]⁺, 430.3 [M+K]⁺, 805.4 [2M+Na]⁺.

SG-53: standard procedure was applied using 2(S)-azido-MCL (20 mg, 0.08 mmol), phenylacetylene (12 μL, 0.12 mmol) in a 1:1 DCM/H₂O mixture (3 mL), copper sulfate pentahydrate (26 mg, 0.12 mmol) and sodium ascorbate (104 mg, 0.52 mmol) to obtain the desired product as a colorless oil (10 mg, 37% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.36-1.42 (m, 4H), 1.89-1.97 (m, 2H), 2.03-2.14 (m, 3H), 2.35 (d, 1H, J=16.5 Hz), 2.50-2.58 (m, 1H), 2.67-2.77 (m, 2H), 2.92 (d, 1H, J=10.5 Hz), 3.85 (t, 1H, J=10.5 Hz), 4.93-5.02 (m, 2H), 5.48 (d, 1H, J=3.0 Hz), 6.21 (d, 1H, J=3.5 Hz), 7.34 (t, 1H, J=7.0 Hz), 7.43 (t, 2H, J=7.5 Hz), 7.65 (s, 1H), 7.83 (d, 2H, J=7.5 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 21.0, 22.9, 29.9, 30.8, 38.1 47.1, 55.0, 59.0, 80.1, 83.3, 118.9, 120.0, 125.7 (2C), 128.2, 128.3, 128.9 (2C) 130.3, 138.0, 140.8, 148.1, 169.3; MS (ESI) calcd for C₂₃H₂₅N₃O₃ m/z: 391.47; found: 392.3 [M+H]⁺, 414.3 [M+Na]⁺, 430.3 [M+K]⁺, 805.4 [2M+Na]⁺.

SG-54: standard procedure was applied using 2(S)-azido-MCL (15 mg, 0.06 mmol) and TPP (12 mg, 0.06 mmol) to obtain the desired product as a colorless oil (2 mg, 14% yield); ¹H NMR (500 MHz, CDCl₃): δ=1.16-1.29 (m, 4H), 1.44 (d, 2H, J=17.0 Hz), 1.602 (s, 1H), 1.75 (d, 2H, J=3.6 Hz), 1.90-1.93 (m, 3H), 2.12 (s, 1H), 2.17 (s, 1H), 2.55 (s, 1H), 2.58 (s, 1H), 3.00 (s, 1H), 3.24 (s, 1H), 5.03 (s, 1H), 5.62 (s, 1H), 6.28 (s, 1H); ¹³C NMR (126 MHz, CDCl₃) δ 18.4, 25.6, 28.3, 33.2, 48.5, 52.9, 55.0, 61.4, 78.9, 82.0, 120.6, 121.7, 127.8, 137.2, 170.5; MS (ESI) calcd for C₁₅H₂₁NO₃ m/z: 263.34; found: 264.4 [M+H]⁺, 286.3 [M+Na]⁺.

SG-55: standard procedure was applied using 14-azido-MCL (30 mg, 0.12 mmol) and TPP (24 mg, 0.12 mmol) to obtain the desired product as a colorless oil (8 mg, 23% yield). ¹H NMR (500 MHz, CDCl₃): δ=110-1.22 (m, 2H), 1.27 (d, 1H, J=10.5 Hz), 1.43 (s, 1H), 1.51 (s, 1H), 1.60-1.66 (m, 1H), 1.68-2.00 (m, 2H), 2.13 (qd, 1H, J₁=12.8, J₂=11.1 Hz), 2.40-2.55 (m, 1H), 2.95-3.05 (m, 2H), 3.27-3.36 (m, 1H), 4.60 (t, 1H, J=10.5 Hz), 5.17-5.28 (m, 1H); ¹³C NMR (126 MHz, CDCl₃) δ 25.8, 27.0, 30.1, 32.4, 40.4, 47.9, 50.1, 58.4, 80.6, 81.7, 121.5, 137.2, 138.9, 140.0, 170.1; MS (ESI) calcd for C₁₅H₂₁NO₃ m/z: 263.34; found: 264.2 [M+H]⁺, 286.3 [M+Na]⁺, 302.3 [M+K]⁺.

SG-62: standard procedure was applied using 14-amino MCL (10 mg, 0.04 mmol), DCC (6 mg, 0.06 mmol), triethylamine (8 μL, 0.12 mmol) and benzyl alcohol (4 mg, 0.06 mmol) to obtain the desired product as yellowish oil (2 mg, 18% yield). ¹H NMR (500 MHz, CDCl₃): 0.80 (s, 1H), 1.20 (s, 3H), 1.30 (dt, 1H, J₁=12.5, J₂=7.0 Hz), 1.55 (dt, 1H, J₁=12.5, J₂ 6.9 Hz), 1.61-1.68 (m, 1H), 1.72-1.78 (m, 1H), 1.85-1.90 (m, 1H), 1.96 (dt, 1H, J₁=12.5, J₂=7.0 Hz), 2.17-2.22 (m, 2H), 2.24-2.30 (m, 1H), 2.50 (d, 1H, J=10.6 Hz), 2.95-3.04 (m, 1H), 3.85 (s, 2H), 4.70 (d, 1H, J=0.6 Hz), 5.55 (dd, 1H, J₁=1.9, J₂=0.8 Hz), 6.32 (dd, 1H, J₁=1.9, J₂=0.8 Hz), 7.37 (t, 2H, J=7.4 Hz), 7.44-7.48 (m, 1H), 7.68 (dd, 2H, J₂=7.5, J₂ 1.4 Hz); ¹³C NMR (126 MHz, CDCl₃) δ 25.8, 27.0, 31.2, 34.3, 37.5, 44.9, 49.9, 58.6, 80.2, 80.9, 120.6, 128.4 (2C), 131.5, 134.7 (2C), 139.4 (2C), 141.2, 143.0, 169.9, 170.7; MS (ESI) calcd for C₂₂H₂₅NO₄ m/z: 367.45; found: 390.2 [M+Na]⁺, 757.5 [2M+Na]⁺.

5.10 Example 10: Synthesis of C2,C13- and C14,C13-Disubstituted Micheliolide Derivatives

This example describes and demonstrates the preparation of compounds of general formula V according to the methods provided herein. In particular, it demonstrates how disubstituted micheliolide derivatives, such as 2,13-disubstituted micheliolide derivatives, can be prepared via chemoenzymatic functionalization of position C2 followed by chemical functionalization of position C13 (FIG. 7 ). Analogously, compounds of general formula VI can be prepared via chemoenzymatic functionalization of position C14 followed by similar procedures for C13 functionalization.

It is well known that the α-methylene-γ-lactone in parthenolide exhibits electrophilic reactivity and that the C13 site in this molecule can thus undergo Michael addition with nucleophilic reagents such as, for example, amine- or thiol-containing reagents. In particular, primary and secondary amines readily add to this site of the molecule (C13) under standard reaction conditions to yield C13-substituted amine-adducts (Guzman, Rossi et al. 2006; Nasim and Crooks 2008; Neelakantan, Nasim et al. 2009). Although this type of modification was not found to lead to significant improvements in the anticancer activity of parthenolide, it can be useful to improve its limited water-solubility (Guzman, Rossi et al. 2006; Nasim and Crooks 2008; Neelakantan, Nasim et al. 2009). Here is demonstrated that is possible to apply the same sort of chemistry to micheliolide anologues of general formula I and II, given the presence of a α-methylene-γ-lactone moiety (FIG. 7 ).

Since the chemoenzymatic functionalization at either the C2 or C14 site of micheliolide as described herein are remote with respect to the C13 site. Both C2- and C14-substituted micheliolide analogs can be further modified at position C13, e.g., via nucleophilic addition of an amine reagent to the α-methylene-γ-lactone moiety, to yield C2,C13- and C13,C14-substituted micheliolide analogs within the scope of the invention. An exemplary procedure for the preparation of doubly substituted micheliolide derivatives of this type is provided in FIG. 7 . Because of the presence of basic amino group in these molecules, salt forms of these molecules can be then prepared via addition of an appropriate acid, which could be beneficial to further improve the water solubility and oral bioavailability of these compounds.

To illustrate this aspect of the invention, an improved C2-modified micheliolide derivative, SG-05, was made react with dimethylamine to yield the corresponding dimethylamino adduct SG-13, while two improved C14-modified micheliolide derivatives, SG-08 and SG-11, were reacted in the same way to yield the corresponding dimethylamino derivatives SG-14 and SG-15.

General Conditions for the Synthesis of Dimethylamino Derivative of 2(S)-Azido-Micheliolide and 14-Azido-Micheliolide:

To a solution of a compound of general formula I or II (0.07 mmol) in 10 mL of absolute EtOH under Ar atmosphere was added dimethylamine 2 M in THF (0.21 mmol). The reaction was allowed to stir until completion (ca. 12 hrs.). After removal of the solvent under reduced pressure, the dimethylamino-derivate product was isolated by silica gel flash chromatography (eluting mixture from 100% EtOAc to 1% MeOH in EtOAc).

SG-13: standard procedure was applied using SG-05 (6 mg, 0.014 mmol) and dimethylamine 2.0 M in MeOH (8 μL, 0.015 mmol) to obtain the desired product as a yellowish oil (7 mg, 99% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.33 (s, 3H), 1.38 (dd, 1H, J=11.0, 23.3 Hz), 1.68 (s, 3H), 1.98 (dd, 1H, J=8.7, 12.5 Hz), 2.13-2.25 (m, 1H), 2.27 (s, 6H), 2.36 (t, 1H, J=14.2 Hz), 2.43 (dt, 1H, J=5.6, 11.5 Hz), 2.58 (dd, 2H, J=7.8, 12.7 Hz), 2.63 (dd, 2H, J=6.5, 13.0 Hz), 2.75 (dd, 2H, J=4.9, 13.0 Hz), 3.02 (d, 1H, J=12.6 Hz), 3.87 (t, 1H, J=10.2 Hz), 5.83 (t, 1H, J=7.4 Hz), 7.70 (d, 2H, J=8.2 Hz), 8.13 (d, 2H, J=8.1 Hz); ¹³C NMR (126 MHz, CDCl₃) δ=24.03, 24.24, 27.20, 36.15, 44.64, 45.40, 45.96 (2C), 49.69, 58.01, 58.26, 74.58, 83.67, 114.68, 120.26, 124.92, 125.46, 129.92 (2C), 130.70, 133.23, 134.39, 139.61, 165.05, 176.57; ¹⁹F NMR (376 MHz, CDCl₃): δ=−0.44; MS (ESI) calcd for C₂₅H₃₀F₃NO₅ m/z: 481.51; found: 482.4 [M+H]⁺.

SG-14: standard procedure was applied using SG-08 (16 mg, 0.032 mmol) and dimethylamine 2.0 M in MeOH (18 μL, 0.035 mmol) to obtain the desired product as a yellowish oil (17 mg, 99% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.20-1.30 (m, 1H), 1.33 (s, 3H), 1.77-1.90 (m, 2H), 2.08 (dd, 1H, J=11.1, 22.6 Hz), 2.17-2.24 (m, 2H), 2.27 (s, 6H), 2.44 (dd, 4H, J=5.1, 12.7 Hz), 2.59-2.68 (m, 2H), 2.71-2.78 (m, 2H), 3.85 (t, 1H, J=10.3 Hz), 4.81 (dd, 2H, J=11.5, 44.0 Hz), 7.89 (s, 2H), 7.99 (s, 1H); ¹³C NMR (126 MHz, CDCl₃) δ=22.82, 27.09, 29.33, 31.58, 38.08, 44.43, 45.87 (2C), 51.15, 57.86, 58.61, 69.45, 80.05, 83.04, 121.66, 123.90, 128.85, 129.28, 129.66, 130.99, 133.39, 133.76, 134.64, 141.60, 165.83, 176.66; ¹⁹F NMR (376 MHz, CDCl₃): δ=−0.46, 2.68; MS (ESI) calcd for C₂₆H₂₉F₆NO₅ m/z: 549.51; found: 550.2 [M+H]⁺, 1099.3 [2M+H]⁺, 1121.4 [2M+Na]⁺.

SG-15: standard procedure was applied using SG-11 (5 mg, 0.013 mmol) and dimethylamine 2.0 M in MeOH (7 μL, 0.014 mmol) to obtain the desired product as a yellowish oil (5 mg, 99% yield). ¹H NMR (500 MHz, CDCl₃): δ=1.18-1.32 (m, 1H), 1.34 (s, 3H), 1.78-1.92 (m, 3H), 2.10 (dd, 4H, J=9.3, 22.9 Hz), 2.15-2.29 (m, 4H), 2.41 (td, 2H, J=6.1, 11.7 Hz), 2.49 (dd, 1H, J=4.7, 18.6 Hz), 2.64 (ddd, 2H, J=7.5, 16.3, 19.4 Hz), 2.70-2.81 (m, 3H), 3.86 (t, 1H, J=10.3 Hz, 1H), 4.76 (s, 2H), 7.12 (t, 2H, J=8.6 Hz), 7.99-8.08 (m, 2H); ¹³C NMR (126 MHz, CDCl₃) δ=22.92, 27.21, 29.19, 29.82, 31.18, 38.28, 44.46, 46.04 (2C), 51.34, 58.09, 58.64, 67.72, 80.14, 83.30, 115.52, 115.69, 125.77, 130.32, 132.10 (2C), 132.29, 140.02, 165.64; ¹⁹F NMR (376 MHz, CDCl₃): δ=−43.03; MS (ESI) calcd for C₂₄H₃₀FNO₅ m/z: 431.50; found: 432.4 [M+H]⁺, 863.5 [2M+H]⁺, 885.5 [2M+Na]⁺.

5.11 Example 11: Antileukemic Activity of the Micheliolide Derivatives

The micheliolide derivatives described in the examples above have been found to possess potent activity against various types of leukemias and lymphomas, including acute myelogenous leukemia (AML). The antileukemic activity of the PTL analogs was evaluated using the leukemia cell line M9-ENL1. M9-ENL1 cells are derived from lineage depleted (Lin⁻) human cord blood cells trasduced with a leukemogenic mixed-lineage leukemia (MLL)-eleven-nineteen leukemia (ENL) fusion gene (Barabe, F.; Kennedy, J. A.; Hope, K. J.; Dick, J. E. Science 2007, 316, 600.). Injected in NOD/SCID mice, M9-ENL1 cells develop a rapid and fatal pro-B cell acute lymphoblastic leukemia (ALL) disease (McDermott, S. P.; Eppert, K.; Notta, F.; Isaac, M.; Datti, A.; Al-Awar, R.; Wrana, J.; Minden, M. D.; Dick, J. E. Blood 2012, 119, 1200; Barabe, F.; Kennedy, J. A.; Hope, K. J.; Dick, J. E. Science 2007, 316, 600). These cells show an enrichment of embryonic and B-cell progenitor gene sets and exhibit the hallmarks and gene expression patters typical of leukemia stem cells (McDermott, S. P.; Eppert, K.; Notta, F.; Isaac, M.; Datti, A.; Al-Awar, R.; Wrana, J.; Minden, M. D.; Dick, J. E. Blood 2012, 119, 1200.). To measure the compound activity on M9-ENL1, cells were treated for 24 hours in the presence or in the absence of the MCL analog at 20 μM (FIG. 8 ), followed by measurement of cell viability using Annexin-V and 7-amino-actinomycin (7-AAD) stains. Half-maximal lethal concentration (LC₅₀) values were obtained from the resulting dose-dependent cell viability curves after normalization to untreated controls (FIG. 9 ). Using this assay, several of the novel MCL analogs disclosed herein were found to exhibit significantly improved antileukemic activity compared to the parent molecule MCL (FIGS. 8 and 9 ). In particular, MCL analogs such as SG-05, SG-52, SG-53, and SG-59 exhibited LD₅₀ values in the low micromolar range, that is nearly 7-fold lower than that of MCL. The most promising MCL analogs were selected for further testing against patient-derived primary AML specimens (FIG. 10 ). Across all the AML specimens tested, the MCL analogs showed improved cytotoxicity compared to the MCL, demonstrating the beneficial effect of the C2- or C14-functionalizations toward enhancing the antileukemic activity of this molecule.

Experimental Procedures.

Biological activity studies were performed using cell-based assays with human leukemia cells (M9-ENL1). Primary AML speciments were obtained with informed consent from volunteer donors. In some cases, cells were cryopreserved in freezing medium of Iscove modified Dulbecco medium (IMDM), 40% fetal bovine serum (FBS), and 10% dimethylsulfoxide (DMSO) or in CryoStor CS-10 (VWR, West Chester, Pa.). Cells were cultured in serum-free medium (SFM) 19 for 1 hour before the addition of parthenolide or its derivatives. Apoptosis assays were performed as described in (Guzman, Neering et al. 2001). Briefly, after 24 hours of treatment, cells were stained for the surface antibodies CD38-allophycocyanin (APC), CD34-PECy7, and CD123-phycoerythin (Becton Dickinson, San Jose, Calif.) for 15 minutes. Cells were washed in cold PBS and resuspended in 200 of annexin-V buffer (0.01 M HEPES/NaOH, 0.14 M NaCl, and 2.5 mM CaCl₂). Annexin-V-fluorescein isothiocyanate (FITC) and 7-aminoactinomycin (7-AAD; Molecular Probes, Eugene, Oreg.) were added, and the tubes were incubated at room temperature for 15 minutes then analyzed on a BD LSRII flow cytometer (BD Biosciences, San Jose, Calif.). Analyses for phenotypically described stem cell subpopulations were performed by gating CD34⁺/CD38⁻ populations. Viable cells were scored as Annexin-V negative/7-AAD negative. The percent viability data provided are normalized to untreated control specimens.

5.12 Example 12: Anticancer Activity of the Micheliolide Derivatives

The micheliolide derivatives described in the examples above have been found to possess potent activity against various types of human cancer cells, including prostate cancer (PC3), neuroblastoma (SK-N-MC), breast cancer (MDA-MB-231), lung cancer (A549), cervical cancer (HeLa), skin cancer (SK-MEL-2), and brain cancer cells (U343MG). The anticancer activity of the compounds was determined using a conventional MTT assay, which measures cell viability upon incubation of the cells with the compounds. Using this assay, many of the MCL analogs were found to exhibit significantly (2- to >10-fold) improved anticancer activity compared to MCL, as determined based on the higher reduction in cancer cell viability upon incubation with the compound at the fixed concentration of 20 μM (FIGS. 11-16 ). Notably, some of the MCL analogs were found to possess a broad anticancer activity profile, being highly active (>70-90% reduction in cell viability) against multiple cancer cell lines (e.g., SG-16). Other MCL analogs, on the other hand, show cancer type-specificity, being highly active only against a subset of the cancer cell lines tested (e.g., SG-35). Overall, these results demonstrate the importance of the C2- and C14-functionalizations for enhancing and modulating the anticancer activity of MCL and obtaining MCL analogs with more promising properties as therapeutic agents.

Experimental Procedures.

All cancer cell lines were maintained in a 37° C. humidified incubator with 5% CO₂. A549, MDA-MB-231, PC-3, SK-N-MC, HeLa, and SK-MEL-2 cells were cultured in DMEM medium (Gibco) supplemented with 10% FBS (Gibco) and 100 I.U./ml penicillin-streptomycin (Sigma). Adherent cells were dissociated using Accutase (Millipore). Adherent cells were seeded in a 96-well plate at a density of 500-10,000 cells per well in 90 μl complete DMEM media. Suspension cells were seeded in conical 96-well plates (Nunc) at a density of 30,000 cells per well in 90 ul of complete α-MEM media devoid of phenol red indicator. The plates were incubated in a humidified incubator for 15 hours prior to treatment. PTL analogs were prepared as concentrated stocks (10 mM) in DMSO and stored at −30° C. Prior to testing, the analogs were diluted into complete cell culture medium and the media was supplemented with sterile DMSO (10% of final volume). For the initial cytotoxicity screening, the compounds were added to the cells in 10 μl aliquots to give a final concentration of 10 μM parthenologs and 1% DMSO (n=5). Following a 24-hour incubation, the culture media from the adherent cell plates (e.g., HeLa, A549) was aspirated and replaced with 100 μl of 1 mg/ml Thiazolyl Blue Tetrazolium Bromide (MTT, Sigma) in complete culture medium devoid of phenol red. After incubation at 37° C. for 3 hours, the plates were centrifuged (4000 rpm, 5 minutes), the media was removed and 100 ul of DMSO was added to solubilize the formazan product. The resulting OD was measured at 550 nm using a multi-well plate reader (Tecan).

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The present invention is not to be limited in scope by the specific embodiments described herein. Indeed, various modifications of the invention in addition to those described herein will become apparent to those skilled in the art from the foregoing description. Such modifications are intended to fall within the scope of the appended claims.

While embodiments of the present disclosure have been particularly shown and described with reference to certain examples and features, it will be understood by one skilled in the art that various changes in detail may be effected therein without departing from the spirit and scope of the present disclosure as defined by claims that can be supported by the written description and drawings. Further, where exemplary embodiments are described with reference to a certain number of elements it will be understood that the exemplary embodiments can be practiced utilizing either less than or more than the certain number of elements.

All references cited herein are incorporated herein by reference in their entirety and for all purposes to the same extent as if each individual publication, patent or patent application was specifically and individually indicated to be incorporated by reference in its entirety for all purposes.

The citation of any publication is for its disclosure prior to the filing date and should not be construed as an admission that the present invention is not entitled to antedate such publication by virtue of prior invention. 

What is claimed is:
 1. A compound of one of general formula (A) and general formula (B), or a pharmaceutically acceptable salt thereof,

A is ═CH₂ or —CH₂R* wherein R* is an amino acid residue bonded to the A methylene via a nitrogen or sulfur atom; or R* is —NR¹R², —NR¹C(O)R², —NR¹CO₂R², or —SR¹, wherein R¹ and R² are independently selected from the group consisting of H and an optionally substituted alkyl, alkenyl, or alkynyl group, an optionally substituted heteroalkyl, heteroalkenyl, or heteroalkynyl group, an optionally substituted aryl group, an optionally substituted heteroaryl group, or an optionally substituted heterocyclic group; or R* is —NR′R², wherein R¹ and R² optionally together with the nitrogen atom form an optionally substituted 5-12 membered ring, the ring optionally comprising at least one heteroatom or group selected from the group consisting of —CO—, —SO—, —SO₂—, and —PO—; L is —O—, —NH—, —NHC(O)—, —OC(O)—, —OC(O)NH—, —S—, —SO—, —SO₂—, —PO—, —OCH₂—, or a chemical bond connecting the carbon atom to Y; and Y represents an optionally substituted alkyl, alkenyl, or alkynyl group, an optionally substituted heteroalkyl, heteroalkenyl, or heteroalkynyl group, an optionally substituted aryl group, an optionally substituted heteroaryl group, or an optionally substituted heterocyclic group, wherein -L-Y together with the carbon atom at position C2 optionally forms carbonyl; or Y is absent and L represents a halogen atom, an azido group (—N₃), an optionally substituted triazole group, or a group —NR³R⁴, where R³ represents a hydrogen atom or an optionally substituted alkyl, alkenyl, or alkynyl group; R⁴ represents an optionally substituted alkyl, alkenyl, alkynyl, aryl, or heteroaryl group; or where R³ and R⁴ are connected together to form an optionally substituted heterocyclic group; M is —O— or —OC(O)— and X represents a hydrogen atom, an optionally substituted alkyl, alkenyl, or alkynyl group, an optionally substituted heteroalkyl, heteroalkenyl, or heteroalkynyl group, an optionally substituted aryl group, an optionally substituted heteroaryl group, or an optionally substituted heterocyclic group.
 2. The compound of claim 1, wherein A is ═CH₂ or CH₂R*, where R* is selected from the group consisting of methylamino (—NH(CH₃)), dimethylamino (—N(CH₃)₂), methylethylamino (— N(CH₃)(CH₂CH₃)), methylpropylamino (—N(CH₃)(CH₂CH₂CH₃)), methylisopropylamino (—(CH₃)(CH₂(CH₃)₂), (—N(CH₃)(CH₂CH₂OH), pyrrolidine, piperidine, 4-methylpiperidine, 1-phenylmethanamine (—NCH₂Ph), and 2-phenylethanamine (—NCH₂CHPh); M is —O—, or —OC(O) —; X is hydrogen, —(C₆-C₁₀) aryl, —(5-14 membered) heteroaryl, (C₁-C₆) alkyl, —N(CH₃)₂—(C₆-C₁₀) aryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; and either (a) L is —OC(O)—; Y is —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, —(C₁-C₆) alkyl, —CH₂—(C₆-C₁₀) aryl, or —NH—(C₆-C₁₀) aryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; or (b) L is —O—; Y is —C(O)—(C₆-C₁₀) aryl, —C(O)— -(5-14 membered) heteroaryl, —CH₂—(C₆-C₁₀) aryl, —C(O)—NH—(C₆-C₁₀) aryl, or —(C₁-C₆) alkyl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen.
 3. The compound of claim 2, wherein Y is —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, or —NH—(C₆-C₁₀) aryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, halogen, phenyl, and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂; M is —O—, or —OC(O)—; X is hydrogen, —(C₆-C₁₀) aryl, -(5-14 membered) heteroaryl, each of which is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; and L is —OC(O)— or —O—.
 4. The compound of claim 1, wherein -L-Y is azide, -(5-14 membered) heteroaryl, amino, halogen, —NH—C(O)—(C₆-C₁₀) aryl, wherein -(5-14 membered) heteroaryl is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂; M is —O—; X is hydrogen, or —C(O)—(C₆-C₁₀) aryl, wherein —C(O)—(C₆-C₁₀) aryl is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen.
 5. The compound of claim 4, wherein -L-Y is -(5-14 membered) heteroaryl, halogen, wherein -(5-14 membered) heteroaryl is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen; A is ═CH₂; X is hydrogen, or —C(O)—(C₆-C₁₀) aryl, wherein —C(O)—(C₆-C₁₀) aryl is optionally substituted with 1 to 3 substituents selected from the group consisting of —CF₃, —N(CH₃)₂, —CH₃, halogen, phenyl and phenyl substituted with 1 to 2 substituents selected from —CF₃ and halogen.
 6. The compound of claim 1, wherein L is —OC(O)—; Y is selected from the group consisting of phenyl, 4-pyridyl, (4-dimethylamino)phenyl, para-, meta-, and ortho-fluoro-phenyl, para-, meta-, and ortho-trifluoromethyl-phenyl, (2,4-bis-trifiuoromethyl)phenyl, (3,5-bis-trifluoromethyl)phenyl, 1- and 2-naphthyl, 3-N-methyl-indolyl, 5-(4-chlorophenyl)isoxazolyl, 2-(4-bromophenyl)furanyl, 2-(2-(trifluoromethyl)phenyl)furanyl, and thiophene; A is ═CH₂ or —CH₂R*, where R* is selected from the group consisting of methylamino (—NH(CH₃)), dimethylamino (—N(CH3)2), methylethylamino (—N(CH₃)(CH₂CH₃)), methylpropylamino (—N(CH₃)(CH₂CH₂CH₃)), methylisopropylamino (—(CH₃)(CH₂(CH₃)₂), (—N(CH₃)(CH₂CH₂OH), pyrrolidine, piperidine, 4-methylpiperidine, 1-phenylmethanamine (—NCH₂Ph), and 2-phenylethanamine (—NCH₂CHPh); and either (a) M is —OC(O)— and X is selected from the group consisting of phenyl, 4-pyridyl, (4-dimethylamino)phenyl, para-, meta-, and ortho-fluoro-phenyl, para-, meta-, and ortho-trifluoromethyl-phenyl, (2,4-bis-trifiuoromethyl)phenyl, (3,5-bis-trifluoromethyl)phenyl, 1- and 2-naphthyl, 3-N-methyl-indolyl, 5-(4-chlorophenyl)isoxazolyl, 2-(4-bromophenyl)furanyl, 2-(2-(trifluoromethyl)phenyl)furanyl, and thiophene; or (b) M is —O— and X represents a hydrogen atom.
 7. The compound of claim 1, wherein L is —O—; Y is selected from the group consisting of (phenyl)methyl, (4-pyridyl)methyl, (4-dimethylaminophenyl)methyl, (para-, meta-, and ortho-fluoro-phenyl)methyl, (para-, meta-, and ortho-trifluoromethyl-phenyl)methyl, (2,4-bis-trifluoromethyl-phenyl)methyl, (3,5-bis-trifluoromethyl-phenyl)methyl, (naphthyl)methyl, (3-N-methyl-indolyl)methyl, (5-(4-chlorophenyl)isoxazolyl)methyl, (2-(4-bromophenyl)furanyl)methyl, (2-(2-(trifluoromethyl)phenyl)furanyl)methyl, methyl(thiophene) and —CH(Ar′)COOR′ group, where Ar′ is selected from the group consisting of phenyl, 4-pyridyl, (4-dimethylamino)phenyl, para-, meta-, and ortho-fluoro-phenyl, para-, meta-, and ortho-trifluoromethyl-phenyl, (2,4-bis-trifluoromethyl)phenyl, (3,5-bis-trifluoromethyl)phenyl, 1- and 2-naphthyl, 3-N-methyl-indolyl, 5-(4-chlorophenyl)isoxazolyl, 2-(4-bromophenyl)furanyl, 2-(2-(trifluoromethyl)phenyl)furanyl, and thiophene group, and R′ is selected from the group consisting of methyl, ethyl, propyl, isopropyl, tert-butyl, benzyl, 2-morpholinoethyl, 2-morpholinoethyl, 2-(piperidin-1-yl)ethyl, and 2-(pyrrolidin-1-yl)ethyl, M is —O—; X represents a hydrogen atom; and A is ═CH₂ or —CH₂R*, where R* is selected from the group consisting of methylamino (—NH(CH₃)), dimethylamino (—N(CH₃)₂), methylethylamino (—N(CH₃)(CH₂CH₃)), methylpropylamino (—N(CH₃)(CH₂CH₂CH₃)), methylisopropylamino (—(CH₃)(CH₂(CH₃)₂), —N(CH₃)(CH₂CH₂OH), pyrrolidine, piperidine, 4-methylpiperidine, 1-phenylmethanamine (—NCH₂Ph), and 2-phenylethanamine (—CH₂CH₂Ph).
 8. A method for inhibiting cancer cell growth in a mammal, the method comprising the step of administering to the mammal afflicted with cancer an amount of a compound of claim 1 effective to inhibit the growth of the cancer cells.
 9. A method for reducing or controlling an inflammatory condition in a mammal, the method comprising the step of administering to the mammal in need thereof, an amount of a compound of claim 1 effective to reduce or control the condition.
 10. A method comprising administering an effective amount of a compound of claim 1 to a patient having acute myeloid leukemia (AML), chronic myeloid leukemia (CML), acute lymphoblastic leukemia (ALL), mantle cell lymphoma (MCL), or large B-cell lymphoma.
 11. A method for treating bone marrow for human bone marrow transplant treatment of leukemia in a patient, comprising the step of treating bone marrow with a compound of claim 1 prior to reintroducing bone marrow into the patient.
 12. A method for inhibiting angiogenesis in a patient in need thereof, the method comprising the step of administering to the patient an effective amount of a compound of claim
 1. 13. A method comprising administering an effective amount of a compound of claim 1 to a patient with a tumor.
 14. The method of claim 13, wherein the tumor is a prostate cancer, a brain cancer, a neuroblastoma, a lung cancer, a breast cancer, a skin cancer, a cervical cancer, a colon cancer, an ovary cancer, or a pancreatic cancer. 